FDA NDC Directory · JSON-LD · Markdown

Lamivudine

NDC 68180-602 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205217
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLAMIVUDINE (150 mg/1)
Marketing started20150325
Package count0

External sources

Source: openFDA. Public-domain (CC0).