FDA NDC Directory · JSON-LD · Markdown

Famciclovir

NDC 64980-349 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091114
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMCICLOVIR (125 mg/1)
Marketing started20110321
Package count1

External sources

Source: openFDA. Public-domain (CC0).