VALSARTAN AND HYDROCHLOROTHIAZIDE

Product NDC

70518-0925

11-digit product format

705180925

Labeler code

70518

Product ID

70518-0925_6181887b-a0d5-6d93-e053-2991aa0a14e2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

valsartan and hydrochlorothiazide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA206083

Marketing category

ANDA

Marketing start

2017-12-29

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