FDA NDC Directory · JSON-LD · Markdown

Famciclovir

NDC 73190-092 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAvKARE
Marketing categoryAbbreviated NDA (generic) · App ANDA202438
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMCICLOVIR (250 mg/1)
Marketing started20260721
Package count1

External sources

Source: openFDA. Public-domain (CC0).