NDC 33342-077 – Valsartan and Hydrochlorothiazide

Valsartan 320 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC33342-077

Product details

Brand name
Valsartan and Hydrochlorothiazide
Generic name
Valsartan and Hydrochlorothiazide
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203145
Marketed since
April 19, 2013
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
33342-077-1090 TABLET, FILM COATED in 1 BOTTLE (33342-077-10)Apr 19, 2013
33342-077-15500 TABLET, FILM COATED in 1 BOTTLE (33342-077-15)Apr 19, 2013

Other Valsartan and Hydrochlorothiazide products