NDC 31722-748 – Valsartan

Valsartan 320 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 4 recalls

Product NDC31722-748

Product details

Brand name
Valsartan
Generic name
Valsartan
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203311
Marketed since
January 5, 2015
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Valsartan →

Package NDC codes (5)

Package NDCDescriptionSince
31722-748-05500 TABLET, FILM COATED in 1 BOTTLE (31722-748-05)Jan 5, 2015
31722-748-3030 TABLET, FILM COATED in 1 BOTTLE (31722-748-30)Jan 5, 2015
31722-748-3110 TABLET, FILM COATED in 1 BLISTER PACK (31722-748-31)Jan 5, 2015
31722-748-32100 TABLET, FILM COATED in 1 BLISTER PACK (31722-748-32)Jan 5, 2015
31722-748-9090 TABLET, FILM COATED in 1 BOTTLE (31722-748-90)Jan 5, 2015

Recalls mentioning this NDC

Other Valsartan products