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Our Products

  1. Pharmaceuticals Tablets 40 Products available
  2. Vaccines 29 Products available
  3. Medicines Tonics And Drugs 27 Products available
  4. Antibiotic Drugs 13 Products available
  5. Pharmaceutical Raw Materials 10 Products available
  6. Catalysts And Absorbents 10 Products available
  7. Pharmaceutical Capsules 9 Products available
  8. Drugs 6 Products available
  9. Pharmaceutical Medicine 6 Products available
  10. Anti Inflammatory Drugs 5 Products available
  11. Antihistamines 5 Products available
  12. Industrial Chemicals 4 Products available
  13. Gastrointestinal Drug 4 Products available
  14. Industrial Acid 3 Products available
  15. Anti Infective Agent 3 Products available
  16. Eye Drops 3 Products available
  17. Antibacterial Drugs 3 Products available
  18. Anti Diabetic Drugs 3 Products available
  19. Anti Hiv Medicines 3 Products available
  20. Antacid Drugs 2 Products available
  21. Anti Asthma Drug 2 Products available
  22. Anti Cancer Medicine 2 Products available
  23. Ores And Minerals 2 Products available
  24. Analgesics 2 Products available
  25. Pharmaceutical Chemical 2 Products available
  26. Arthritic Drugs 1 Products available
  27. Antiviral Drugs 1 Products available
  28. Cardiovascular Medication & Drugs 1 Products available
  29. Active Pharmaceutical Ingredients 1 Products available
  30. Nervous & Brain System Drugs 1 Products available
  31. Health Care Products 1 Products available
  32. Dietary Supplements 1 Products available
  33. Api Intermediate 1 Products available
  34. Skin Cream 1 Products available
  35. Others Products 30 Products available

Our Products

We offer a complete product range of Ranitidine Tablets, Zhewitra 40 Mg, Gefitinib Tablets, Pramipexole and Agomelatine

Agomelatine

  • Shelf Life 5 years if sealed and store away from direct sun light.
  • Grade Standard IP / BP / USP
  • Therapeutic Category Antidepressant
  • CAS No 138112-76-2
  • COA Available
  • MSDS Available
  • Formula C15H17NO2
  • Molar mass 243.301 g/mol
  • Bioavailability 1%
  • Protein binding 95%
  • Metabolism hepatic (90% CYP1A2 and 10% CYP2C9)
  • Biological half-life 1-2 hours Excretion -Renal (80%, mostly as metabolites)
  • Storage Stored in a clean, cool, dry area; keep away from moisture and strong, direct light/heat

Additional Information:

Packaging Details : 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.

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Amikacin Sulphate

  • Grade IP / BP / USP
  • Therapeutic Category Antibiotic
  • CAS No 37517-28-5
  • Other Name Amikacin
  • COA Available
  • MSDS Available
  • English name Amikacin
  • Molecular Formula C22H43N5O13
  • Molecular Weight 585.6025
  • Shelf Life 5 years if sealed and store away from direct sun light.

Storage:Stored in a clean, cool, dry area; keep away from moisture and strong, direct light/heat

Additional Information:

Packaging Details : 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.

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Isoflurane Vaporizer

  • Product Name Isoflurane Vaporizer
  • Packaging Type 30 ml, 100 ml, 250 ml
  • Production Capacity 1 million/month
  • Trade Name Forane
  • Pack Insert/Leaflet Yes
  • Therapeutic use Generic Drugs, Branded Medicines, Anaesthetic

Isoflurane, sold under the trade nameForaneamong others, is ageneral anestheticIt can be used to start or maintainanesthesia.Often another medication, however, is used to start anesthesia due to airway irritation with isofluraneIt is used byinhalation.

Side effects include adecreased effort to breathe(respiratory depression), low blood pressure, andirregular heartbeat.Serious side effects may includemalignant hyperthermiaandhigh blood potassium.It should not be used in people with a history of malignant hyperthermia either in themselves or their family members.

It is unknown if use duringpregnancyis safe for the baby; however, use during acesarean sectionappears to be okay.Isoflurane is in thehalogenated etherfamily of medication.

Isoflurane was approved for medical use in the United States in 1979.It is on theWorld Health Organization's List of Essential Medicines, the most effective and safe medicines needed in ahealth system.

Additional Information:

Packaging Details : 30 ml, 100 ml, 250 ml

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Amphotericin B

  • Grade IP / BP / USP
  • CAS No. 1397-89-3
  • Shelf Life 5 years if sealed and store away from direct sun light.
  • Therapeutic Category Antifungal
  • COA Available
  • MSDS Available
  • Storage Stored in a clean, cool, dry area; keep away from moisture and strong, direct light/heat

Side effects:

  • Fever and chills
  • headache
  • increased or decreased urination
  • irregular heartbeat
  • muscle cramps or pain
  • nausea
  • pain at the place of injection

 

Additional Information:

Packaging Details : 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.

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Nimesulide Tablets

  • Product Name Nimesulide Tablets
  • Trade Name Nicip, Nicip DS, Nise, Sulide
  • Available Strength 50 mg, 100 mg, 200 mg
  • Available Combination Nimesulide + Paracetamol tablet, Nimesulide +Serratiopeptidase tablet
  • Packing 10X10 Tablets/Box
  • Pack Insert/Leaflet Yes
  • Therapeutic use painkiller, NSAID, Analgesic, Antipyretic, Anti Inflammatory
  • Production Capacity 10 million tablet/month

what is nimesulide?

nimesulide tabletis a medicine that is used for the treatment ofacute pain, rheumatoid arthritis, osteoarthritis, dysmenorrhea, thrombophlebitis and other conditions.

nimesulide tablet contains nimesulide as an active ingredient.

nimesulide tablet works by blocking the production of prostaglandins thereby relieving pain and inflammation.

detailed information related to nimesulide tablet's uses, composition, dosage, side effects and reviews is listed below.

nimesulide tablet uses

nimesulide tabletis used for the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms:

acute pain

rheumatoid arthritis

osteoarthritis

dysmenorrhea

thrombophlebitis

nimesulide tablet working, mechanism of action and pharmacology

nimesulide tablet improves the patient's condition by performing the following functions:

blocking the production of prostaglandins thereby relieving pain and inflammation.

nimesulide tablet - composition and active ingredients

nimesulide tabletis composed of the following active ingredients (salts)

nimesulide (100 mg)

please note that this medicine may be available in various strengths for each active ingredient listed above.

nimesulide tablet - side-effects

the following is a list of possible side effects that may occur from all constituting ingredients ofnimesulide tablet. This is not a comprehensive list. These side effects are possible, but do not always occur. Some of the side effects may be rare but serious. Consult your doctor if you observe any of the following side effects, especially if they do not go away.

dizziness

erosive stomatitis

gastritis

hypersensitivity reactions

nausea

constipation

nimesulide tablet - precautions & how to use

before using this drug, inform your doctor about your current list of medications, over the counter products (e.g. Vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e.g. Pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below.

can cause infertility in women

do not take medicine if you are allergic to nimesulide

do not use if you have gastric ulceration

Additional Information:

Payment Terms : L/C, T/T,

Packaging Details : 10X10 Tablets/Box

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Benzhexol

  • Grade IP / BP / USP
  • Therapeutic Category Antiparkinsonian
  • CAS No 52-49-3
  • Other Name Trihexyphenidyl
  • COA Available
  • MSDS Available
  • Shelf Life 5 years if sealed and store away from direct sun light.
  • Storage Stored in a clean, cool, dry area; keep away from moisture and strong, direct light/heat

 

Additional Information:

Packaging Details : 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.

Technical Specification

Item Specifications Results
Appearance White or creamy white crystalline powder Conforms
Identification Positive Positive
Acidity 5.5 to 6.2 5.25
Related substances ≤0.5%(single) 0.0019
  ≤1.0%(total) 0.0031
Loss on drying ≤0.5% 0.0027
Sulphated ash ≤0.1% 0.0002
Assay 98.0 to 101.0% 0.9979
Conclusion The results conforms with BP standards
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Ranitidine Tablets

  • Product Name Ranitidine Tablets
  • Trade Name Aciloc, Zinetac, Zantac
  • Available Strength 150 mg, 300 mg
  • Available Combination Ranitidine+ Domperidone tablet
  • Packing 10X10 Tablets/Box
  • Pack Insert/Leaflet Yes
  • Therapeutic use Antiulcer, Antacid
  • Production Capacity 10 million tablet/month

What is Ranitidine?

Ranitidine Tablet is a medicine that is used for the treatment of Benign Duodenal Ulcer,  Gastric Ulcer, Inflammation Of The Esophagus, Acid Peptic Disease and other conditions.

Ranitidine Tablet contains Ranitidine as an active ingredient.

Ranitidine Tablet works by blocking the action of histamine on proteins.

Detailed information related to Ranitidine Tablet's uses, composition, dosage, side effects and reviews is listed below.

 

Ranitidine Tablet Uses

Ranitidine Tablet is used for the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms:

·         Benign Duodenal Ulcer

·         Gastric Ulcer

·         Inflammation Of The Esophagus

·         Acid Peptic Disease

 

Ranitidine Tablet Working, Mechanism of Action and Pharmacology

Ranitidine Tablet improves the patient's condition by performing the following functions:

·         Blocking the action of histamine on proteins.

 

Ranitidine Tablet - Composition and Active Ingredients

Ranitidine Tablet is composed of the following active ingredients (salts)

·         Ranitidine (150 MG)

Please note that this medicine may be available in various strengths for each active ingredient listed above.

Ranitidine Tablet - Side-effects

The following is a list of possible side effects that may occur from all constituting ingredients of Ranitidine Tablet. This is not a comprehensive list. These side effects are possible, but do not always occur. Some of the side effects may be rare but serious. Consult your doctor if you observe any of the following side effects, especially if they do not go away.

·         Swelling Of Lips

·         Headache

·         Diarrhea

·         Very Low Blood Pressure

·         Chest Pain

·         Increase Of Serum Creatinine In The Blood

 

Ranitidine Tablet - Precautions & How to Use

Before using this drug, inform your doctor about your current list of medications, over the counter products (e.g. vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e.g. pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below.

·         Do not take this medication if you are allergic to it

·         Pregnant or planning to get pregnant

Additional Information:

Packaging Details : 10X10 Tablets/Box

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Candesartan Cilexetil

  • Grade IP / BP / USP
  • Storage Stored in a clean, cool, dry area; keep away from moisture and strong, direct light/heat
  • Therapeutic Category Anti hypertensive
  • CAS No 145040-37-5
  • 145040-37-5 Candesartan
  • COA Available
  • MSDS Available
  • Available 5 years if sealed and store away from direct sun light.

 

Additional Information:

Packaging Details : 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.

Technical Specification

ITEMS SPECIFICATIONS RESULTS
Description White or almost white
crystalline powder
Almost white crystalline powder
Solubility Freely soluble in Chloroform
Sparingly soluble in anhydrous ethanol
Slightly soluble in acetonitrile
Practically insoluble in water
 
Conforms
HPLC
UV
IR
Must conform to reference standard
Must conform to reference standard
Must conform to reference standard
Conforms
Conforms
Conforms
Loss on drying Not more than 0.5% 0.0006
Chloride Not more than 0.035% <0.035%
Residue on ignition Not more than 0.1% 0.0003
Heavy metals Not more than 10 ppm <10 ppm
Ethyl candesartan
Desethyl candesartan
Other Individual impurity
Total impurities
Not more than 0.3%
Not more than 0.3%
Not more than 0.1%
Not more than 1.0%
0.11%
0.15%
0.05%
0.37%
Ethanol
Acetone
Ethyl acetate
Dichloromethane
N, N-Dimethylformamide
n-Heptane
Acetic acid
Not more than 0.5%
Not more than 0.5%
Not more than 0.5%
Not more than 0.06%
Not more than 0.088%
Not more than 0.5%
Not more than 0.3%
Conforms
0.004%
Conforms
Conforms
Conforms
Conforms
Conforms
Assay 98.0~102.0% 0.9865






































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Albendazole & Ivermectin Suspension

  • Product Name Albendazole & Ivermectin Suspension
  • Trade Name Wormectol, Bandy Plus
  • Packing 5ml Bottle , 10ml Bottle
  • Pack Insert/Leaflet Yes
  • Therapeutic use Anthelmintic, Antiprotozoal, Antiparasitic
  • Production Capacity 1 million syrup/month
What is Albendazole & Ivermectin?

Albendazole & Ivermectin Suspension is a medicine that is used for the treatment of Infections Caused By Roundworm, Infections Caused By Tapeworm, Infections Caused By Pinworm, Parasitic Infection Of Skin, Parasitic Infection Of Hair, Inflammatory Diseases and other conditions.

Albendazole & Ivermectin Suspension contains Albendazole, and Ivermectin as active ingredients.

Albendazole & Ivermectin Suspension works by keeping away the worm from absorbing sugar; killing the parasite by paralyzing it;

Detailed information related to Albendazole & Ivermectin Suspension's uses, composition, dosage, side effects and reviews is listed below.

Albendazole & Ivermectin Suspension Uses

Albendazole & Ivermectin Suspension is used for the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms:

·         Infections Caused By Roundworm

·         Infections Caused By Tapeworm

·         Infections Caused By Pinworm

·         Parasitic Infection Of Skin

·         Parasitic Infection Of Hair

·         Inflammatory Diseases

·         Threadworm Infections

·         Pinworms Infections

·         Parasitic Nematode Worms Intestine Infections

Albendazole & Ivermectin Suspension Working, Mechanism of Action and Pharmacology

Albendazole & Ivermectin Suspension improves the patient's condition by performing the following functions:

·         Keeping away the worm from absorbing sugar.

·         Killing the parasite by paralyzing it.

Albendazole & Ivermectin Suspension - Composition and Active Ingredients

Albendazole & Ivermectin Suspension is composed of the following active ingredients (salts)

·         Albendazole (200 MG)

·         Ivermectin (1.5 MG)

Please note that this medicine may be available in various strengths for each active ingredient listed above.

Albendazole & Ivermectin Suspension - Side-effects

The following is a list of possible side-effects that may occur from all constituting ingredients of Albendazole & Ivermectin Suspension. This is not a comprehensive list. These side-effects are possible, but do not always occur. Some of the side-effects may be rare but serious. Consult your doctor if you observe any of the following side-effects, especially if they do not go away.

·         Fatigue

·         Sore Throat

·         Shortness Of Breath

·         Nausea

·         Pale Skin

·         Abdominal Pain

Albendazole & Ivermectin Suspension - Precautions & How to Use

Before using this drug, inform your doctor about your current list of medications, over the counter products (e.g. vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e.g. pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side-effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below.

·         Consult your doctor in case of renal impairment

·         Have concurrent loa loa infection, suffering from brain problems, bleeding disorder, or asthma

·         Liver disease

·         Pregnant or breastfeeding

·         Should be taken empty stomach with water

·         Take fluid and fiber rich diet

Additional Information:

Packaging Details : 5ml Bottle , 10ml Bottle

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Gefitinib Tablets

  • Packaging Type 30 Tablets/Bottle , 10X10 Tablets/Bottle
  • Product Name Gefitinib Tablets
  • Trade Name Geftinat, Iressa, Geffy
  • Available Strength 250 mg
  • Pack Insert/Leaflet Yes
  • Therapeutic use Anti Cancer
  • Production Capacity 1 million tablet/month
What is Gefitinib?

Gefitinib Tablet is a medicine that is used for the treatment of Non-Small Cell Lung Cancer After Failure Of Platinum And Docetaxel Chemotherapies and other conditions.

Gefitinib Tablet contains Gefitinib as an active ingredient.

Gefitinib Tablet works by blocking a protein to inhibit spread and growth of cancer cells.

Detailed information related to Gefitinib Tablet's uses, composition, dosage, side effects and reviews is listed below.

Gefitinib Tablet Uses

Gefitinib Tablet is used for the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms:

·         Non-Small Cell Lung Cancer After Failure Of Platinum And Docetaxel Chemotherapies

Gefitinib Tablet Working, Mechanism of Action and Pharmacology

Gefitinib Tablet improves the patient's condition by performing the following functions:

·         Blocking a protein to inhibit spread and growth of cancer cells.

Gefitinib Tablet - Composition and Active Ingredients

Gefitinib Tablet is composed of the following active ingredients (salts)

·         Gefitinib (250 MG)

Please note that this medicine may be available in various strengths for each active ingredient listed above.

Gefitinib Tablet - Side-effects

The following is a list of possible side-effects that may occur from all constituting ingredients of Gefitinib Tablet. This is not a comprehensive list. These side-effects are possible, but do not always occur. Some of the side-effects may be rare but serious. Consult your doctor if you observe any of the following side-effects, especially if they do not go away.

·         Red Or Sore Eyelids

·         Nausea

·         Red Or Sore Mouth

·         Inflammation Of The Liver

·         Dehydration

·         Red Or Itchy Eyes

Gefitinib Tablet - Precautions & How to Use

Before using this drug, inform your doctor about your current list of medications, over the counter products (e.g. vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e.g. pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side-effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below.

·         Avoid if you are pregnant or breastfeeding

·         Be careful while driving or using tools or machines

·         Do not take antacids 2 hours before or 1 hour after taking gefitinib

·         Inform your doctor if you are taking a medicine containing warfarin as an active substance

·         Take the tablet at about the same time each day

 

Additional Information:

Packaging Details : 30 Tablets/Bottle , 10X10 Tablets/Bottle

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Desvenlafaxine Succinate

  • Grade IP / BP / USP
  • MF C16H25NO2.C4H6O4.H2O
  • Therapeutic Category Antidepressant
  • CAS No 386750-22-7
  • COA Available
  • MSDS Available
  • MW 399.48
  • Shelf Life 5 years if sealed and store away from direct sun light.
  • Storage Stored in a clean, cool, dry area; keep away from moisture and strong, direct light/heat

 

Additional Information:

Packaging Details : 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.

Technical Specification

Item Specifications Results
Appearance White or whitish powder Conform
Water 4.5%-5.5% 0.0514
Heavy metal max10ppm 8ppm
Residue on Ignition max0.2% 0.0002
Assay ≥98.5% 99.49.0%
Conclusion The results conforms with enterprise standards
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Imatinib Capsules

  • Product Name Imatinib Capsules
  • Trade Name Imatib, Gleevec, Glivec
  • Available Strength 100 mg, 400 mg
  • Packing 10X10 Capsules/Box
  • Pack Insert/Leaflet Yes
  • Therapeutic use Anti Cancer
  • Production Capacity 1 million capsule/month
What is Imatinib?

Imatinib Capsule is a medicine that is used for the treatment of Blood Cancer,  Gastrointestinal Stromal Tumors,  Bone Marrow Cancer,  Blood Cells Disorder, Hypereosinophilic Syndrome, Mast Cell Disease and other conditions.

Imatinib Capsule contains Imatinib Mesylate as an active ingredient.

Imatinib Capsule works by preventing cancer cells multiplication across the body.

Detailed information related to Imatinib Capsule's uses, composition, dosage, side effects and reviews is listed below.

Imatinib Capsule Uses

Imatinib Capsule is used for the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms:

·         Blood Cancer

·         Gastrointestinal Stromal Tumors

·         Bone Marrow Cancer

·         Blood Cells Disorder

·         Hypereosinophilic Syndrome

·         Mast Cell Disease

Imatinib Capsule Working, Mechanism of Action and Pharmacology

Imatinib Capsule improves the patient's condition by performing the following functions:

·         Preventing cancer cells multiplication across the body.

Imatinib Capsule - Composition and Active Ingredients

Imatinib Capsule is composed of the following active ingredients (salts)

·         Imatinib Mesylate

Please note that this medicine may be available in various strengths for each active ingredient listed above.

Imatinib Capsule - Side-effects

The following is a list of possible side-effects that may occur from all constituting ingredients of Imatinib Capsule. This is not a comprehensive list. These side-effects are possible, but do not always occur. Some of the side-effects may be rare but serious. Consult your doctor if you observe any of the following side-effects, especially if they do not go away.

·         Chills

·         Fever

·         Swelling Due To Fluid Retention

·         Headache

·         Blurred Vision

·         Sore Throat

Imatinib Capsule - Precautions & How to Use

Before using this drug, inform your doctor about your current list of medications, over the counter products (e.g. vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e.g. pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side-effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below.

·         Cardiac disease or increased risk for congestive heart failure

·         Do not drive or operate heavy machinery

·         Do not give this drug to children without consultation

·         Pregnant or planning to get pregnant

·         Renal and hepatic impairment

Additional Information:

Packaging Details : 10X10 Capsules/Box

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Fluconazole Powder

  • Shelf Life 5 years if sealed and store away from direct sun light.
  • Grade IP / BP / USP
  • Appearance white crystalline powder
  • Therapeutic Category Antifungal
  • CAS No 86386-73-4
  • COA Available
  • MSDS Available
  • Storage Stored in a clean, cool, dry area; keep away from moisture and strong, direct light/heat

Additional Information:

Packaging Details : 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.

Technical Specification

Item Specification
Identification UV Conforms
IR Conforms
Related substance Impurity A: ≤0.2%
Impurity B ≤0.10%
Impurity C: ≤0.2%
Any other impurity:≤0.10%
Total of other impurities:≤0.3%
Total impurities:≤1.5%
Loss on drying,% ≤ 0.5%
Residue on ignition ≤ 0.1%
Appearance of solubility Conforms
Assay(on dried basis) 99.00% to 102.00%
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Flunarizine

  • Grade IP / BP / USP
  • Therapeutic Category Antihistamines
  • CAS No 52468-60-7
  • Other Name Flunarizine dihydrochloride
  • MSDS Available
  • Formula C26H28Cl2F2N2
  • MW 477.42
  • Boiling point 511.3°C at 760 mmHg
  • Flash point 263°C
  • Appearance white crystalline powder
  • Appearance of solution clear and colourless
  • Moisture 1.0% max
  • 1.0% max 0.5% max
  • Heavy metals 10ppm max
  • Assay 99% min
  • Shelf Life 5 years if sealed and store away from direct sun light.
  • Storage Stored in a clean, cool, dry area; keep away from moisture and strong, direct light/heat

 

Additional Information:

Packaging Details : 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.

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Dexamethasone Eye Drops

  • Product Name Dexamethasone Eye Drops
  • Trade Name Maxidex, Dexoren
  • Available Strength 0.1% w/v
  • Pack Insert/Leaflet Yes
  • Therapeutic use Steroid, Anti Inflammatory
  • Production Capacity 1 million drop/month

what is dexamethasone eye drops?

dexamethasone eye dropsis a medicine that is used for the treatment of skin inflammation, allergy, ulcerative colitis, breathing problems, lupus vulgaris or lupus erythematosus, arthritisand other conditions.

dexamethasone eye drops contains dexamethasone as an active ingredient.

dexamethasone eye drops works by preventing late phase allergic reactions by preventing release of chemicals responsible for allergy.

detailed information related to dexamethasone eye drops's uses, composition, dosage, side effects and reviews is listed below.

dexamethasone eye drops uses

dexamethasone eye dropsis used for the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms:

skin inflammation

allergy

ulcerative colitis

breathing problems

lupus vulgaris or lupus erythematosus

arthritis

dexamethasone eye drops working, mechanism of action and pharmacology

dexamethasone eye drops improves the patient's condition by performing the following functions:

preventing late phase allergic reactions by preventing release of chemicals responsible for allergy.

dexamethasone eye drops - composition and active ingredients

dexamethasone eye dropsis composed of the following active ingredients (salts)

dexamethasone (0.5mg/ml)

please note that this medicine may be available in various strengths for each active ingredient listed above.

dexamethasone eye drops - side-effects

the following is a list of possible side effects that may occur from all constituting ingredients ofdexamethasone eye drops. This is not a comprehensive list. These side effects are possible, but do not always occur. Some of the side effects may be rare but serious. Consult your doctor if you observe any of the following side effects, especially if they do not go away.

depressed

labile mood

suicidal thoughts

menstrual irregularity

swelling due to fluid retention

potassium loss

dexamethasone eye drops - precautions & how to use

before using this drug, inform your doctor about your current list of medications, over the counter products (e.g. Vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e.g. Pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below.

do not stop using dexamethasone suddenly

do not use it if you have a fungal infection, stomach or duodenal ulcer, kidney or liver problems

do precaution if you have high blood pressure, heart disease or you have recently had a heart attack

  • available combination :dexamethasone + neomycin, dexamethasone + ciprofloxacin, dexamethasone + moxifloxacin, dexamethasone + gentamicin, dexamethasone + chloramphenicol, dexamethasone + tobramycin, dexamethasone + gatiflox

Additional Information:

Packaging Details : 5ml, 10ml

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Ketorolac Eye Drops

  • Product Name Ketorolac Eye Drops
  • Trade Name Toradol, Acular and Sprix
  • Available Strength 0.5% w/v
  • Available Combination Moxifloxacin & Ketorolac Eye Drops
  • Packing 5 ml, 10 ml
  • Pack Insert/Leaflet Yes
  • Therapeutic use NSAID, Anti Inflammatory
  • Production Capacity 1 million drop/month
what is ketorolac?

ketorolac eye drops is a medicine that is used for the treatment ofpostoperative pain, inflammation of the eye, central eye retina disorder, painless disorder of retina associated with cataract extraction, visual loss after cataract surgery, pain and photophobia in patients undergoing eye surgeryand other conditions.

ketorolac eye drops contains ketorolac tromethamine as an active ingredient.

ketorolac eye drops works by blocking the effect of chemicals causing pain.

detailed information related to ketorolac eye drops's uses, composition, dosage, side effects and reviews is listed below.

ketorolac eye drops uses

ketorolac eye drops is used for the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms:

postoperative pain

inflammation of the eye

central eye retina disorder

painless disorder of retina associated with cataract extraction

visual loss after cataract surgery

pain and photophobia in patients undergoing eye surgery

ketorolac eye drops working, mechanism of action and pharmacology

ketorolac eye drops improves the patient's condition by performing the following functions:

blocking the effect of chemicals causing pain.

ketorolac eye drops - composition and active ingredients

ketorolac eye drops is composed of the following active ingredients (salts)

ketorolac tromethamine

please note that this medicine may be available in various strengths for each active ingredient listed above.

ketorolac eye drops - side-effects

the following is a list of possible side effects that may occur from all constituting ingredients ofketorolac eye drops. This is not a comprehensive list. These side effects are possible, but do not always occur. Some of the side effects may be rare but serious. Consult your doctor if you observe any of the following side effects, especially if they do not go away.

gastrointestinal ulcer

bleeding

perforation

drowsiness

rash

bronchospasm

ketorolac eye drops - precautions & how to use

before using this drug, inform your doctor about your current list of medications, over the counter products (e.g. Vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e.g. Pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below.

have eye infection, dry eyes, ulcer on the surface of the eye, bleeding tendency or stomach ulcers, diabetes, rheumatoid arthritis, or asthma

symptoms of bleeding in the stomach or intestines

Additional Information:

Packaging Details : 5 ml, 10 ml

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Ondansetron Tablets

  • Product Name Ondansetron Tablets
  • Trade Name Emeset, Zofran, Ondisolv
  • Available Strength 2 mg , 4 mg, 8 mg
  • Packing 10X10Tablets/Box
  • Pack Insert/Leaflet Yes
  • Therapeutic use Antiemetic, Anti Vomiting
  • Production Capacity 10 million tablet/month

what is ondansetron?

ondansetron tabletis a medicine that is used for the treatment ofnausea and vomiting caused by chemotherapy or radiotherapyand other conditions.

ondansetron tablet contains ondansetron as an active ingredient.

ondansetron tablet works by works on small intestine and brain that controls vomiting or nausea.

detailed information related to ondansetron tablet's uses, composition, dosage, side effects and reviews is listed below.

ondansetron tablet uses

ondansetron tabletis used for the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms:

nausea and vomiting caused by chemotherapy or radiotherapy

ondansetron tablet working, mechanism of action and pharmacology

ondansetron tablet improves the patient's condition by performing the following functions:

works on small intestine and brain that controls vomiting or nausea.

ondansetron tablet - composition and active ingredients

ondansetron tabletis composed of the following active ingredients (salts)

ondansetron (4 mg)

please note that this medicine may be available in various strengths for each active ingredient listed above.

ondansetron tablet - side-effects

the following is a list of possible side effects that may occur from all constituting ingredients ofondansetron tablet. This is not a comprehensive list. These side effects are possible, but do not always occur. Some of the side effects may be rare but serious. Consult your doctor if you observe any of the following side effects, especially if they do not go away.

uneven heartbeats

headache

low blood pressure leading to fainting or dizziness

unusual body movements or shaking

changes to results of some liver function tests

constipation

ondansetron tablet - precautions & how to use

before using this drug, inform your doctor about your current list of medications, over the counter products (e.g. Vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e.g. Pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below.

do not chew or crush the tablets

do not take double dose for making up forgotten dose

do not use if you are allergic to omeprazole

Additional Information:

Payment Terms : L/C, T/T,

Packaging Details : 10X10Tablets/Box

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Ondansetron Suspension

  • Product Name Ondansetron Suspension
  • Trade Name Zofran, Ondisolv
  • Available Strength 2 mg/ 5ml
  • Packing 30 ml Bottle
  • Pack Insert/Leaflet Yes
  • Therapeutic use Antiemetic, Anti Vomiting
  • Production Capacity 1 million syrup/month
What is Ondansetron?

Ondansetron Suspension is a medicine that is used for the treatment of Nausea And Vomiting Caused By Chemotherapy Or Radiotherapy and other conditions.

Ondansetron Suspension contains Ondansetron as an active ingredient.

Ondansetron Suspension works by works on small intestine and brain that controls vomiting or nausea.

Detailed information related to Ondansetron Suspension's uses, composition, dosage, side effects and reviews is listed below.

Ondansetron Suspension Uses

Ondansetron Suspension is used for the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms:

·         Nausea And Vomiting Caused By Chemotherapy Or Radiotherapy

Ondansetron Suspension Working, Mechanism of Action and Pharmacology

Ondansetron Suspension improves the patient's condition by performing the following functions:

·         Works on small intestine and brain that controls vomiting or nausea.

Ondansetron Suspension - Composition and Active Ingredients

Ondansetron Suspension is composed of the following active ingredients (salts)

·         Ondansetron (2 MG)

Please note that this medicine may be available in various strengths for each active ingredient listed above.

Ondansetron Suspension - Side-effects

The following is a list of possible side-effects that may occur from all constituting ingredients of Ondansetron Suspension. This is not a comprehensive list. These side-effects are possible, but do not always occur. Some of the side-effects may be rare but serious. Consult your doctor if you observe any of the following side-effects, especially if they do not go away.

·         Uneven Heartbeats

·         Headache

·         Low Blood Pressure Leading To Fainting Or Dizziness

·         Unusual Body Movements Or Shaking

·         Changes To Results Of Some Liver Function Tests

·         Constipation

Ondansetron Suspension - Precautions & How to Use

Before using this drug, inform your doctor about your current list of medications, over the counter products (e.g. vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e.g. pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side-effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below.

·         Do not chew or crush the tablets

·         Do not take double dose for making up forgotten dose

·         Do not use if you are allergic to omeprazole

Additional Information:

Packaging Details : 30 ml Bottle

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Ambroxol Terbutaline

  • Product Name Ambroxol Terbutaline & Guaiphenesin Syrup
  • Packaging Type 60ml Bottle
  • Production Capacity 1 million syrup/month
  • Trade Name Brored
  • Pack Insert/Leaflet Yes
  • Therapeutic use Antiasthmatic, Antitussive, Bronchodilator
Description

 

What is Ambroxol Terbutaline & Guaiphenesin?

Ambroxol Terbutaline & Guaiphenesin Syrup is a medicine that is used for the treatment of Respiratory Diseases,  Cough, Congestion,  Common Cold,  Bronchitis, Breathing Illnesses and other conditions.

Ambroxol Terbutaline & Guaiphenesin Syrup contains Ambroxol Hydrochloride, Guaiphenesin, Menthol, and Terbutaline Sulphate as active ingredients.

Ambroxol Terbutaline & Guaiphenesin Syrup works by thinning the chest mucus; thinning the mucus in the air passages; relaxing and opening the airways; temporarily relieving minor pain;

Detailed information related to Ambroxol Terbutaline & Guaiphenesin Syrup's uses, composition, dosage, side effects and reviews is listed below.

Ambroxol Terbutaline & Guaiphenesin Syrup Uses

Ambroxol Terbutaline & Guaiphenesin Syrup is used for the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms:

·         Respiratory Diseases

·         Cough

·         Congestion

·         Common Cold

·         Bronchitis

·         Breathing Illnesses

·         Reversible Airway Obstructive Diseases

·         Uncomplicated Premature Labor

·         Pain In Arthritis

·         Pain In Shoulder Joint

·         Pain In Tendons

·         Pain In Muscle Strains Or Sprains

·         Back Pain

·         Bruising

Ambroxol Terbutaline & Guaiphenesin Syrup Working, Mechanism of Action and Pharmacology

Ambroxol Terbutaline & Guaiphenesin Syrup improves the patient's condition by performing the following functions:

·         Thinning the chest mucus.

·         Thinning the mucus in the air passages.

·         Relaxing and opening the airways.

·         Temporarily relieving minor pain.

Ambroxol Terbutaline & Guaiphenesin Syrup - Composition and Active Ingredients

Ambroxol Terbutaline & Guaiphenesin Syrup is composed of the following active ingredients (salts)

·         Ambroxol Hydrochloride (15 MG)

·         Guaiphenesin (50 MG)

·         Terbutaline Sulphate (1.25 MG)

·         Menthol (1 MG)

Please note that this medicine may be available in various strengths for each active ingredient listed above.

Ambroxol Terbutaline & Guaiphenesin Syrup - Side-effects

The following is a list of possible side-effects that may occur from all constituting ingredients of Ambroxol Terbutaline & Guaiphenesin Syrup. This is not a comprehensive list. These side-effects are possible, but do not always occur. Some of the side-effects may be rare but serious. Consult your doctor if you observe any of the following side-effects, especially if they do not go away.

·         Gastric Ulceration

·         Stomach Pain

·         Loose Motions

·         Vomiting

·         Itchy Skin Rash

·         Hypersensitivity

Ambroxol Terbutaline & Guaiphenesin Syrup - Precautions & How to Use

Before using this drug, inform your doctor about your current list of medications, over the counter products (e.g. vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e.g. pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side-effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below.

·         Alcohol consumption

·         Asthma

·         Avoid use of this drug during first trimester of pregnancy

·         Breastfeeding or planning to get pregnant

·         Do not drive or operate machinery

·         Emphysema

 

Additional Information:

Packaging Details : 60ml Bottle

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Dextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup

  • Product Name Dextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup
  • Trade Name Dilo-DX
  • Packing 100 ml Bottle
  • Pack Insert/Leaflet Yes
  • Therapeutic use Antiasthmatic, Antitussive, Bronchodilator
  • Production Capacity 1 million syrup/month
What is Dextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup?

Dextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup Syrupis a medicine that is used for the treatment ofDry Cough, Painful Cough, Runny Nose, Sneezing I Itching, Watery Eyes Caused By Allergies, Common Coldand other conditions.

Dextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup Syrup contains Chlorpheniramine Maleate, Dextromethorphan, and Phenylephrine as active ingredients.

Dextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup Syrup works by decreasing activity in the part of the brain that causes coughing; blocking a natural chemical that makes during an allergic rejection; constricting the blood vessels results in decreasing the flow of blood thus relieves nasal congestion;

Detailed information related to Dextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup Syrup's uses, composition, dosage, side effects and reviews is listed below.

Dextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup Syrup Uses

Dextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup Syrupis used for the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms:

Dry Cough

Painful Cough

Runny Nose

Sneezing I Itching

Watery Eyes Caused By Allergies

Common Cold

Flu

Allergies Due To Food

Hypotensive Conditions

Nasal Decongestant

Eye Mydriasis

Intraocular Tension

Dextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup Syrup Working, Mechanism of Action and Pharmacology

Dextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup Syrup improves the patient's condition by performing the following functions:

Decreasing activity in the part of the brain that causes coughing.

Blocking a natural chemical that makes during an allergic rejection.

Constricting the blood vessels results in decreasing the flow of blood thus relieves nasal congestion.

Dextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup Syrup - Composition and Active Ingredients

Dextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup Syrupis composed of the following active ingredients (salts)

Dextromethorphan (10 MG)

Chlorpheniramine Maleate (2 MG)

Phenylephrine (5 MG)

Please note that this medicine may be available in various strengths for each active ingredient listed above.

Dextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup Syrup - Side-effects

The following is a list of possibleside-effectsthat may occur from all constituting ingredients ofDextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup Syrup. This is not a comprehensive list. These side-effects are possible, but do not always occur. Some of the side-effects may be rare but serious. Consult your doctor if you observe any of the following side-effects, especially if they do not go away.

Skin Rashes

Feeling Drowsy

Headache

Breathing Problems

Vomiting

Urge To Vomit

Dextromethorphan Chlorpheniramine Maleate & Phenylephrine Syrup Syrup - Precautions & How to Use

Before using this drug, inform your doctor about your current list of medications, over the counter products (e.g.vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e.g. pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side-effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below.

Allow the dextromethorphan lozenge or disintegrating strip to dissolve in your mouth

Always ask a doctor before giving cough or cold medicine to a child

Avoid smoking and use of

Breastfeeding

Cautiously do exercise in case of elderly, pylori duodenal obstruction, angle-closure glaucoma, epilepsy, renal and hepatic impairment

Consult your doctor if suffering from coronary artery disease

Additional Information:

Payment Terms : L/C, T/T,

Packaging Details : 100 ml Bottle

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Diphenhydramine Ammonium Chloride Sodium Citrate & Menthol Syrup

  • Product Name Diphenhydramine Ammonium Chloride Sodium Citrate & Menthol Syrup
  • Trade Name Benadryl, Cof-Ryl
  • Packing 100 ml Bottle
  • Pack Insert/Leaflet Yes
  • Therapeutic use Antiasthmatic, Antitussive, Bronchodilator
  • Production Capacity 1 million syrup/month
What is Diphenhydramine Ammonium Chloride Sodium Citrate+Menthol?

Diphenhydramine Ammonium Chloride Sodium Citrate & Menthol Syrupis a medicine that is used for the treatment ofCough Relief, Hypochloremia, Metabolic Alkalosis, Pain In Arthritis, Pain In Shoulder Joint, Pain In Tendonsand other conditions.

Diphenhydramine Ammonium Chloride Sodium Citrate & Menthol Syrup contains Ammonium Chloride, Diphenhydramine, Menthol, and Sodium Citrate as active ingredients.

Diphenhydramine Ammonium Chloride Sodium Citrate & Menthol Syrup works by converting the ammonia to urea by the liver; regulating the acid-base balance; temporarily relieving minor pain; regulating the intake of sodium and potassium; blocking the action of histamine during an allergy;

Detailed information related to Diphenhydramine Ammonium Chloride Sodium Citrate & Menthol Syrup's uses, composition, dosage, side effects and reviews is listed below.

Diphenhydramine Ammonium Chloride Sodium Citrate & Menthol Syrup Uses

Diphenhydramine Ammonium Chloride Sodium Citrate & Menthol Syrupis used for the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms:

Cough Relief

Hypochloremia

Metabolic Alkalosis

Pain In Arthritis

Pain In Shoulder Joint

Pain In Tendons

Pain In Muscle Strains Or Sprains

Back Pain

Bruising

Acidity

Gastric Problems

Kidney Stones

Cough

Red Eye

Irritated Eye

Itchy Eyes

Watery Eyes

Sneezing

Diphenhydramine Ammonium Chloride Sodium Citrate & Menthol Syrup Working, Mechanism of Action and Pharmacology

Diphenhydramine Ammonium Chloride Sodium Citrate & Menthol Syrup improves the patient's condition by performing the following functions:

Converting the ammonia to urea by the liver; regulating the acid-base balance.

Temporarily relieving minor pain.

Regulating the intake of sodium and potassium.

Blocking the action of histamine during an allergy.

Diphenhydramine Ammonium Chloride Sodium Citrate & Menthol Syrup - Composition and Active Ingredients

Diphenhydramine Ammonium Chloride Sodium Citrate & Menthol Syrupis composed of the following active ingredients (salts)

Ammonium Chloride (135 MG)

Menthol (0.9 MG)

Sodium Citrate (57 MG)

Diphenhydramine (14 MG)

Please note that this medicine may be available in various strengths for each active ingredient listed above.

Diphenhydramine Ammonium Chloride Sodium Citrate & Menthol Syrup - Side-effects

The following is a list of possibleside-effectsthat may occur from all constituting ingredients ofDiphenhydramine Ammonium Chloride Sodium Citrate & Menthol Syrup. This is not a comprehensive list. These side-effects are possible, but do not always occur. Some of the side-effects may be rare but serious. Consult your doctor if you observe any of the following side-effects, especially if they do not go away.

Pain At The Site Of Injection

Infection At The Site Of Injection

Venous Thrombosis

Phlebitis

Hypervolemia

Metabolic Acidosis

Diphenhydramine Ammonium Chloride Sodium Citrate & Menthol Syrup - Precautions & How to Use

Before using this drug, inform your doctor about your current list of medications, over the counter products (e.g.vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e.g. pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side-effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below.

Avoid alcohol intake

Consult a doctor if you have cardiac failure, hypertension, impaired renal function or peripheral and pulmonary edema

Drink plenty of fluids

Drive or operate machinery

Pregnant, planning to become pregnant or breastfeeding

Taking prescription or nonprescription medicine

Additional Information:

Payment Terms : L/C, T/T,

Packaging Details : 100 ml Bottle

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Ofloxacin

  • Shelf Life 5 years if sealed and store away from direct sun light.
  • Grade Standard IP / BP / USP
  • Therapeutic Category Antibiotic
  • CAS No 82419-36-1
  • COA Available
  • MSDS Available
  • Storage Stored in a clean, cool, dry area; keep away from moisture and strong, direct light/heat

 

Additional Information:

Packaging Details : 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.

Technical Specification

TESTS SPECIFICATION RESULTS
Identification A: IR test
B: UV test
Conform
Description White or yellowish crystalline powder Conform
Specific rotation -10 ~ +10 0.2
Loss on drying % ≤0.2 0.18
Purity Test (HPLC)
A: Individual impurity(%)
B: 9-desfluoro ofloxacin(%)
C: total impurity(%)
 
≤0.3
≤0.2
≤0.5
 
0.21
0.08
0.21
Residue on ignition % ≤0.1 0.06
Heavy Metals % ≤0.001 <0.001
Arsenic ≤1ug/g Conform
Residual Solvents
A: Methanol %
B: Ethanol %
 
≤0.005
≤0.05
 
<0.005
<0.05
Assay % ≥98.5 99.1
Conclusion: Comforms
















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Pramipexole

  • Grade IP / BP / USP
  • Purity 99%
  • Therapeutic Category Antidyskinetic
  • CAS No 104632-26-0
  • Other Name PRAMIPEXOLE DIHYDROCHLORIDE
  • COA Available
  • MSDS Available
  • Molecular formula C10H17N3S
  • Molecular weight 247.788
  • Appearance white powder
  • Shelf Life 5 years if sealed and store away from direct sun light.
  • Storage Stored in a clean, cool, dry area; keep away from moisture and strong, direct light/heat

Additional Information:

Packaging Details : 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.

Technical Specification

Test Items Standard Test Results
Character Off-white to White  Crystalline powder Off-White Crystalline powder
Solubility Soluble in Water and Methanol, slightly soluble in Ethanol (96%),
Almost insoluble in  Dichloromethane
Complies
Identification (1)Specific Rotation -67~-69.5°(on anhydrate basis)
(2)IR: Meets the requirement.
(3) Optical purity Test
(4)Chloride Reaction
-68.8
 
Complies
Complies
Complies
Clarity Clear, not deeper than Y6. Complies
PH 2.8~3.4 3.15
Related Substances Impurity A≤0.15%
Impurity B≤0.15%
Impurity C≤0.15%
Unknown single impurity≤0.1%
Total Impurity≤0.5%
Not detected
0.04%
Not detected
0.05%
0.16%
Impurity D Impurity D≤0. 5% 0.001
Water 4.5%~6.5% 0.049
Heavy metals ≤10ppm Complies
Sulfate Ash ≤0.1% 0.0005
Assay (on anhydrate basis) 99.0%~101.0% 0.998
















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Tazobactam

  • Grade IP / BP / USP
  • Therapeutic Category Penicillins
  • CAS No 89786-04-9
  • COA Available
  • MSDS Available
  • Shelf Life 5 years if sealed and store away from direct sun light.
  • Storage Stored in a clean, cool, dry area; keep away from moisture and strong, direct light/heat

 

Additional Information:

Packaging Details : 25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum.

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Vilitra 60 Mg

  • Min. Order (MOQ) 100 Piece
  • Purity 99.5%
OverviewVilitra 60 mg helps adult males in the treatment of impotence or erectile dysfunction (ED) condition. Erectile dysfunction condition is explained as an inability of achieving and keeping the hard erection enough to complete the sensual playing satisfactorily. Hence, Vilitra is taken during intended lovemaking session that helps a man accomplish and sustain the required hardness in order to fulfill the sensual desire without experiencing the erectile disappointments. Mechanism of action of Vilitra 60 mgVilitra 60 mg is a popular brand that contains generic Vardenafil, which helps in ED treatment. When a man is sensually provoked, his body releases nitric oxide and result in the increased blood flow towards erectile organ for attaining hardness. Therefore, during ED, Vilitra helps in blocking PDE-5 enzyme resulting in the widening of narrowed blood vessels followed with the prevention of cGMP deprivation. Consequently, a man will be capable of accomplishing and keeping the firm erection in action for satisfying the complete sensual intimacy eliminating the erection failure issue. The dosage schedule of Vilitra 60 mgVilitra 60 mg is an orally ingested tablet formulation advised to be taken orally using water and regardless of the food. Hence, the dosage regimen is advised as an oral consumption of a single dose of Vilitra 60 mg at approximate 45minutes prior to the intended lovemaking session with the partner. Sensual arousal is must for the drug to be active within 30minutes of tablet use so that the drug remains active for the next 4-5hours. Hence, more than 1tablet is not suggested on the same day and should be taken only when required with a gap of 24hours between two doses else, an overdose of Vilitra will result in painful or prolonged erection (priapism). Conflicting conditions for the use of Vilitra 60 mgDo not take any medication called nitrates or anything that may have nitrate constituent with Vilitra 60 mg because of the risk of sudden

Additional Information:

Payment Terms : L/C, T/T,

Packaging Details : Medicine Type : Allopathic
Dosage : As per doctor's prescription
Pack Size : 10x10 Tablets
Storage : Cool & Dry Place
Form : Tablets
Strength : 60 mg

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Zhewitra 40 Mg

  • Min. Order (MOQ) 100 Piece
  • Purity 99.5%
DescriptionZhewitra 40mg (Vardenafil Tablets) is a prescription for men's to manage the problem of their erection. Erectile dysfunction is an ailment that makes the males unable to get along to accomplish a strong erection for improved sensual performance. Erection delinquent follows mostly due to narrowing of the blood vessels near the penile region. FunctionZhewitra 40mg shows its result by hampering the action of PDE-5 blocker that aids to lessen the blood vessels and recovers the proper movement of blood to the man reproductive system and accomplishes the desire of sexual intercourse. For better consequences have this drug when you are planning for interaction moment and proceed for physical intercourse. Side EffectsDizzinessStuffy noseNausea or vomitingHeadacheChest painLoss of visionHearing loss

Additional Information:

Payment Terms : L/C, T/T,

Packaging Details : Storage : Cool & Dry Place
Form : Tablets
Strength : 40 mg
Dosage : As per doctor's prescription
Medicine Type : Allopathic
Pack Size : 10 Tablets

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Vega 100 Mg

1 - 100 / Piece Get Latest Price
  • Min. Order (MOQ) 100 Strip
  • Number Of Flower Ed Product
  • Purity 99.5%
  • Dosage Form Tablets
  • Country of Origin India
descriptionvega 100 mg tablet relaxes the smooth muscles present in the wall of blood vessels and helps in increasing the flow of blood in certain specific areas of the body. it is used for the treatment of erection disorders and pulmonary hypertension (high blood pressure of blood vessels connecting the lungs and the heart). useserectile dysfuntion - vega 100 mg tablet is used for the treatment of impotence; where achieving and sustaining an erection is a problem while having sexual intercourse. however, it will work only if there is sexual stimulation.pulmonary arterial hypertension - vega 100 mg tablet is used to treat high blood pressure of arteries present in the lungs and right side of the heart. it also improves exercise capacity in such patients. side effectsheadachesevereflushingbloody noseindigestionseveresleeplessnessdiarrheadizzinessseverebloody and cloudy urinesevereburning, numbness, tingling in the arms and feetseverechanges in visionsevereraresensitivity to lightsevererareprolonged and painful erectionsevererarepainful urination strength : 100 mgstorage : cool & dry placemedicine type : allopathicdosage : as per doctor's prescriptionpack size : 4 tabletsindication : erectile dysfunctionform : tablets

Additional Information:

Payment Terms : L/C, T/T, Western Union,

Packaging Details : By courier

Delivery Time : 5 days

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Betadine Powder

  • Application External use only
  • Packaging Size 30 GM
  • Form Powder
  • Purity 100%
  • Medicine Type Allopathic
  • Storage Cool & Dry Place

What is Betadine?

  • Betadine Powder is used for Wound infection, Wound infections, Abrasions, Minor cuts, Vaginal infection, Blisters, Infection in wounds, Oral hygiene, Burns, Grazes and other conditions. Betadine Powder may also be used for purposes not listed in this medication guide.
  • Betadine Powder contains Povidone Iodine as an active ingredient.
  • Betadine Powder works by liberating iodine in contact with the skin.

Uses :Betadine Powder is used for the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms.

  • Wound infection
  • Wound infections
  • Abrasions
  • Minor cuts
  • Vaginal infection
  • Blisters
  • Infection in wounds
  • Oral hygiene
  • Grazes
  • Burns
  • Oral thrush

Side Effects :The following is a list of possible side-effects that may occur from all constituting ingredients of Betadine Powder. This is not a comprehensive list. These side-effects are possible, but do not always occur. Some of the side-effects may be rare but serious. Consult your doctor if you observe any of the following side-effects, especially if they do not go away.

  • Metabolic acidosis
  • Hypernatremia
  • Impairment of renal function
  • Conjunctival hyperemia
  • Superficial punctate keratitis
  • Hypersensitivity reactions
  • Yellow coloration of the conjunctiva
  • Anaphylactic reaction
  • Hypothyroidism in neonates
  • Reversible transient brown coloration

Precautions & How to Use : Before using Betadine Powder, inform your doctor about your current list of medications, over the counter products (e.g. vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e.g. pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side-effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below.

  • Consult your doctor if skin rash and itching occurs
  • Do not use povidone iodine solution without consulting the doctor
  • Keep this drug out of reach from children

Additional Information:

Payment Terms : L/C, T/T,

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