Valsartan and Hydrochlorothiazide

Product NDC

68071-2059

11-digit product format

680712059

Labeler code

68071

Product ID

68071-2059_46dfe5ef-4978-34a7-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Valsartan and Hydrochlorothiazide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA203145

Marketing category

ANDA

Marketing start

2013-04-19

Marketing end

0000-00-00

Substance

VALSARTAN; HYDROCHLOROTHIAZIDE

Active strength

320 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