NDC 71335-0567 – Valsartan

Valsartan 80 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC71335-0567

Product details

Brand name
Valsartan
Generic name
Valsartan
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204821
Marketed since
August 31, 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 (4)

Package NDCDescriptionSince
71335-0567-130 TABLET in 1 BOTTLE (71335-0567-1)Nov 22, 2023
71335-0567-290 TABLET in 1 BOTTLE (71335-0567-2)Nov 22, 2023
71335-0567-360 TABLET in 1 BOTTLE (71335-0567-3)Nov 22, 2023
71335-0567-428 TABLET in 1 BOTTLE (71335-0567-4)Nov 22, 2023

Recalls mentioning this NDC

Other Valsartan products