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Famciclovir

NDC 31722-707 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202438
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFAMCICLOVIR (250 mg/1)
Marketing started20140910
Package count5

External sources

Source: openFDA. Public-domain (CC0).