Valsartan and Hydrochlorothiazide

Product NDC

50268-790

11-digit product format

502680790

Labeler code

50268

Product ID

50268-790_6dd20ee1-7314-a4ba-e053-2991aa0a7a5b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Valsartan and Hydrochlorothiazide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

AvPAK

Application

ANDA078946

Marketing category

ANDA

Marketing start

2016-08-01

Marketing end

0000-00-00

Substance

HYDROCHLOROTHIAZIDE; VALSARTAN

Active strength

13 mg/1; mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record