NDC 63629-7890 – Famciclovir

Famciclovir 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC63629-7890

Product details

Brand name
Famciclovir
Generic name
Famciclovir
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202438
Marketed since
September 10, 2014
Listing expires
December 31, 2026
Pharmacologic class
Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Famciclovir →

Package NDC codes (1)

Package NDCDescriptionSince
63629-7890-130 TABLET, FILM COATED in 1 BOTTLE (63629-7890-1)Jan 11, 2019

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