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Darunavir

NDC 70771-1745 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA214085
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDARUNAVIR (600 mg/1)
Marketing started20240501
Package count3

External sources

Source: openFDA. Public-domain (CC0).