Entecavir
-Plant extracts
Entecavir
1.High quality plant extracts;
2.Organic and Natural；
3.Better stability.
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Product information
Production Technology
Produced under ICH Q7 standards with multi-step purification and recrystallization to control impurities. Tablets follow WHO-GMP production with stable dissolution and bioequivalence. Complete stability and pharmacovigilance documents support FDA, EMA, NMPA registration.
Core Advantages
- Prescription antiviral product with stable bulk supply for domestic wholesale and export
- Low impurity, complete DMF, CEP and registration documents for overseas filing
- Flexible order sizes: trial samples, medium bulk and large tender batches with competitive prices
- Standard cold-chain logistics guarantee product activity during transportation
Sales Qualification & Channels
Domestic Market
- Tablets are Class A prescription medicine: Retail requires pharmacy license + doctor prescription; wholesale needs drug distribution license
- API only sold to manufacturers with valid drug production & GMP certificates
Export Market
API for overseas generic tablet factories; finished tablets export to Southeast Asia, Middle East, Africa and Latin America. All shipments support customs clearance with SDS, COA and free sale certificates.
Application Fields
- Prescription oral tablets and oral liquid for chronic hepatitis B treatment
- Raw material for generic antiviral pharmaceutical preparations
- Hospital pharmacies and official medical procurement projects
Storage & Operation
API packed with inner aluminum bag + fiber drum, RH ≤60%, cool dry storage. Tablets sealed in blisters at 20–25°C. Wear dust-proof gloves and masks during weighing and mixing, keep separate from food and cosmetic raw materials.
Our Advantages
Long-term stable stock, full set of test certificates and registration files. Support trial samples and large wholesale orders.
Related raw material link: Glycine
Global compliance standard: FDA Official Portal