NDC 71205-609 – Famciclovir

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

Human Prescription Drug

Product NDC71205-609

Product details

Brand name
Famciclovir
Generic name
Famciclovir
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA201022
Marketed since
January 13, 2012
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 (4)

Package NDCDescriptionSince
71205-609-2121 TABLET, FILM COATED in 1 BOTTLE (71205-609-21)Oct 4, 2021
71205-609-3030 TABLET, FILM COATED in 1 BOTTLE (71205-609-30)Oct 4, 2021
71205-609-6060 TABLET, FILM COATED in 1 BOTTLE (71205-609-60)Oct 4, 2021
71205-609-9090 TABLET, FILM COATED in 1 BOTTLE (71205-609-90)Oct 4, 2021

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