NDC 31722-704 – Valacyclovir

Valacyclovir Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC31722-704

Product details

Brand name
Valacyclovir
Generic name
Valacyclovir
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203047
Marketed since
May 25, 2015
Listing expires
December 31, 2026
Pharmacologic class
Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Valacyclovir →

Package NDC codes (7)

Package NDCDescriptionSince
31722-704-01100 TABLET, FILM COATED in 1 BOTTLE (31722-704-01)May 25, 2015
31722-704-05500 TABLET, FILM COATED in 1 BOTTLE (31722-704-05)May 25, 2015
31722-704-3030 TABLET, FILM COATED in 1 BOTTLE (31722-704-30)May 25, 2015
31722-704-3110 TABLET, FILM COATED in 1 BLISTER PACK (31722-704-31)May 25, 2015
31722-704-3210 TABLET, FILM COATED in 1 BLISTER PACK (31722-704-32)May 25, 2015
31722-704-6060 TABLET, FILM COATED in 1 BOTTLE (31722-704-60)May 25, 2015
31722-704-9090 TABLET, FILM COATED in 1 BOTTLE (31722-704-90)May 25, 2015

Recalls mentioning this NDC

Other Valacyclovir products