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Apigat Apixaban Tablets 2.5mg

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Apigat Apixaban Tablets 5mg

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Description

Description

  • High-quality anticoagulant tablet containing Apixaban 5 mg.
  • Indicated for prevention of stroke & systemic embolism in patients with non-valvular atrial fibrillation, treatment & prevention of deep vein thrombosis (DVT) and pulmonary embolism (PE) & other thromboembolic disorders.
  • Manufactured under WHO-GMP / ISO & regulatory approved facility.
  • Supplied in blister/strip packaging or bottles as per market requirement. Suitable for domestic & export markets.
  • Offers stable shelf life, robust packaging, and complete documentation (COA, GMP certificate, regulatory clearances).
  • Application: Hospitals, clinics, retail pharmacies, institutional procurement, exports.

Specification

Parameter Details
Active Ingredient (Salt) Apixaban 5 mg
Dosage Form Film-coated tablet
Strength 5 mg per tablet
Pack Size e.g., 10 × 10 tablets per blister (or as specified)
Storage Conditions Store in a cool, dry place. Protect from light and moisture.
Shelf Life e.g., 24 months from manufacturing (subject to packing)
Manufacturing Standard WHO-GMP / ISO / Schedule H compliance (as applicable)
Manufacturer [Manufacturer Name & Address]
Country of Origin India
Product Highlights – Effective Factor Xa inhibitor- Oral administration for ease of use- Minimal monitoring compared to older anticoagulants
Regulatory / Quality Sterile from extraneous substances, meets pharmacopeial specifications, complete batch documentation available
Minimum Order Quantity (Specify as per your supply)
Payment Terms / Delivery (Specify: e.g., TT advance, net30, FOB/EXW, Lead time)
Packaging & Labelling (Specify: e.g., blister + box, export carton, cold chain if required)

Usage / Application

  • For use under prescription/medical supervision only.
  • Applicable for hospitals, clinics, retail distribution, institutional supply, export business.
  • Suitable for procurement by wholesalers, distributors, pharmacy chains and export houses.

Precautions & Compliance

  • Prescription only medicine; follow legal/regulatory guidelines for sale and distribution.
  • Ensure compliance with local licensing (Schedule H, etc.) and export regulations if shipping outside India.
  • Manufacturer to provide all regulatory documentation (GMP certificate, COA, stability data, free sale certificate, etc.).

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