Valsartan and Hydrochlorothiazide

Product NDC

70518-0329

11-digit product format

705180329

Labeler code

70518

Product ID

70518-0329_9b26323c-78de-d97f-e053-2a95a90a8c23

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Valsartan and Hydrochlorothiazide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA203145

Marketing category

ANDA

Marketing start

2017-03-17

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

2021-12-31

Current FDA listing

Historical FDA.report record