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TENOFOVIR DISOPROXIL FUMARATE

NDC 64380-714 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nametenofovir disoproxil fumarate
Labeler / ManufacturerStrides Pharma Science Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA090742
Dosage form / routeTABLET · ORAL
Active ingredientsTENOFOVIR DISOPROXIL FUMARATE (300 mg/1)
Marketing started20180126
Package count1

External sources

Source: openFDA. Public-domain (CC0).