NDC 46708-453 – Valsartan and Hydrochlorothiazide

Valsartan 80 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC46708-453

Product details

Brand name
Valsartan and Hydrochlorothiazide
Generic name
Valsartan and Hydrochlorothiazide
Labeler
Alembic Pharmaceuticals Limited
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
46708-453-10100 TABLET, FILM COATED in 1 CARTON (46708-453-10)May 20, 2016
46708-453-3030 TABLET, FILM COATED in 1 BOTTLE (46708-453-30)May 20, 2016
46708-453-71500 TABLET, FILM COATED in 1 BOTTLE (46708-453-71)May 20, 2016
46708-453-9090 TABLET, FILM COATED in 1 BOTTLE (46708-453-90)May 20, 2016

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