FDA NDC Directory · JSON-LD · Markdown

Lamivudine

NDC 33342-002 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA090198
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLAMIVUDINE (300 mg/1)
Marketing started20190502
Package count1

External sources

Source: openFDA. Public-domain (CC0).