NDC 31722-832 – Valganciclovir

Valganciclovir Hydrochloride 450 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC31722-832

Product details

Brand name
Valganciclovir
Generic name
Valganciclovir
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205166
Marketed since
March 18, 2016
Listing expires
December 31, 2026
Pharmacologic class
Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor; Nucleoside Analog Antiviral

Active ingredients

Uses, dosage, side effects and warnings for Valganciclovir →

Package NDC codes (3)

Package NDCDescriptionSince
31722-832-3110 TABLET, FILM COATED in 1 BLISTER PACK (31722-832-31)Mar 18, 2016
31722-832-3210 TABLET, FILM COATED in 1 CARTON (31722-832-32)Mar 18, 2016
31722-832-6060 TABLET, FILM COATED in 1 BOTTLE (31722-832-60)Mar 18, 2016

Recalls mentioning this NDC

Other Valganciclovir products