NDC 43547-313 – Valsartan And Hydrochlorothiazide

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

Human Prescription Drug 5 recalls

Product NDC43547-313

Product details

Brand name
Valsartan And Hydrochlorothiazide
Generic name
valsartan and hydrochlorothiazide
Labeler
Solco Healthcare US, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206083
Marketed since
October 31, 2015
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
43547-313-0330 TABLET, FILM COATED in 1 BOTTLE (43547-313-03)Dec 3, 2021
43547-313-0990 TABLET, FILM COATED in 1 BOTTLE (43547-313-09)Dec 3, 2021
43547-313-50500 TABLET, FILM COATED in 1 BOTTLE (43547-313-50)Dec 3, 2021

Recalls mentioning this NDC

Other Valsartan and Hydrochlorothiazide products