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LAMIVUDINE

NDC 60505-3252 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namelamivudine
Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA091606
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLAMIVUDINE (300 mg/1)
Marketing started20111202
Package count2

External sources

Source: openFDA. Public-domain (CC0).