NDC 62332-081 – Valsartan and Hydrochlorothiazide

Valsartan 160 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC62332-081

Product details

Brand name
Valsartan and Hydrochlorothiazide
Generic name
Valsartan and Hydrochlorothiazide
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA201662
Marketed since
May 20, 2016
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 (4)

Package NDCDescriptionSince
62332-081-10100 TABLET, FILM COATED in 1 BOTTLE (62332-081-10)May 20, 2016
62332-081-3030 TABLET, FILM COATED in 1 BOTTLE (62332-081-30)May 20, 2016
62332-081-71500 TABLET, FILM COATED in 1 BOTTLE (62332-081-71)May 20, 2016
62332-081-9090 TABLET, FILM COATED in 1 BOTTLE (62332-081-90)May 20, 2016

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