Valsartan and Hydrochlorothiazide

Product NDC

68788-6793

11-digit product format

687886793

Labeler code

68788

Product ID

68788-6793_f1d989cc-5c69-4e4d-bf36-6b6ee3b6856f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Valsartan and Hydrochlorothiazide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA203145

Marketing category

ANDA

Marketing start

2016-11-02

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

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record