FDA NDC Directory · JSON-LD · Markdown

Lamivudine

NDC 31722-752 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203260
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLAMIVUDINE (100 mg/1)
Marketing started20140102
Package count4

External sources

Source: openFDA. Public-domain (CC0).