Valsartan and Hydrochlorothiazide

Product NDC

51655-953

11-digit product format

516550953

Labeler code

51655

Product ID

51655-953_4d373996-1f9c-5336-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Valsartan and Hydrochlorothiazide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Northwind Pharmaceuticals

Application

ANDA202519

Marketing category

ANDA

Marketing start

2016-08-12

Marketing end

0000-00-00

Substance

VALSARTAN; HYDROCHLOROTHIAZIDE

Active strength

160 mg/1; mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record