NDC 71335-2154 – Valsartan

Valsartan 160 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2154

Product details

Brand name
Valsartan
Generic name
Valsartan
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203311
Marketed since
June 23, 2021
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Valsartan →

Package NDC codes (7)

Package NDCDescriptionSince
71335-2154-130 TABLET, FILM COATED in 1 BOTTLE (71335-2154-1)Aug 22, 2022
71335-2154-290 TABLET, FILM COATED in 1 BOTTLE (71335-2154-2)Aug 22, 2022
71335-2154-3120 TABLET, FILM COATED in 1 BOTTLE (71335-2154-3)Aug 22, 2022
71335-2154-4180 TABLET, FILM COATED in 1 BOTTLE (71335-2154-4)Aug 22, 2022
71335-2154-528 TABLET, FILM COATED in 1 BOTTLE (71335-2154-5)Aug 22, 2022
71335-2154-660 TABLET, FILM COATED in 1 BOTTLE (71335-2154-6)Aug 22, 2022
71335-2154-7100 TABLET, FILM COATED in 1 BOTTLE (71335-2154-7)Aug 22, 2022

Other Valsartan products