NDC 31722-708 – Famciclovir

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

Human Prescription Drug 1 recall

Product NDC31722-708

Product details

Brand name
Famciclovir
Generic name
Famciclovir
Labeler
Camber Pharmaceuticals, Inc.
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 (5)

Package NDCDescriptionSince
31722-708-01100 TABLET, FILM COATED in 1 BOTTLE (31722-708-01)Sep 10, 2014
31722-708-05500 TABLET, FILM COATED in 1 BOTTLE (31722-708-05)Sep 10, 2014
31722-708-101000 TABLET, FILM COATED in 1 BOTTLE (31722-708-10)Sep 10, 2014
31722-708-3030 TABLET, FILM COATED in 1 BOTTLE (31722-708-30)Sep 10, 2014
31722-708-6060 TABLET, FILM COATED in 1 BOTTLE (31722-708-60)Sep 10, 2014

Recalls mentioning this NDC

Other Famciclovir products