FDA NDC Directory · JSON-LD · Markdown

Famciclovir

NDC 42291-415 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAvKARE
Marketing categoryAbbreviated NDA (generic) · App ANDA077487
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMCICLOVIR (250 mg/1)
Marketing started20210519
Package count1

External sources

Source: openFDA. Public-domain (CC0).