NDC 31722-707 – Famciclovir

Famciclovir 250 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC31722-707

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
31722-707-01100 TABLET, FILM COATED in 1 BOTTLE (31722-707-01)Sep 10, 2014
31722-707-05500 TABLET, FILM COATED in 1 BOTTLE (31722-707-05)Sep 10, 2014
31722-707-101000 TABLET, FILM COATED in 1 BOTTLE (31722-707-10)Sep 10, 2014
31722-707-3030 TABLET, FILM COATED in 1 BOTTLE (31722-707-30)Sep 10, 2014
31722-707-6060 TABLET, FILM COATED in 1 BOTTLE (31722-707-60)Sep 10, 2014

Recalls mentioning this NDC

Other Famciclovir products