FDA NDC Directory · JSON-LD · Markdown

Lamivudine

NDC 67046-1459 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090457
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLAMIVUDINE (150 mg/1)
Marketing started20250206
Package count1

External sources

Source: openFDA. Public-domain (CC0).