NDC 50090-6232 – Valsartan And Hydrochlorothiazide

Valsartan 160 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-6232

Product details

Brand name
Valsartan And Hydrochlorothiazide
Generic name
Valsartan and hydrochlorothiazide
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206083
Marketed since
October 31, 2015
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Valsartan and Hydrochlorothiazide →

Package NDC codes (2)

Package NDCDescriptionSince
50090-6232-090 TABLET, FILM COATED in 1 BOTTLE (50090-6232-0)Nov 17, 2022
50090-6232-130 TABLET, FILM COATED in 1 BOTTLE (50090-6232-1)Nov 17, 2022

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