FDA NDC Directory · JSON-LD · Markdown

Famciclovir

NDC 63629-7890 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA202438
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMCICLOVIR (500 mg/1)
Marketing started20140910
Package count1

External sources

Source: openFDA. Public-domain (CC0).