Valsartan

Product NDC

0591-2170

11-digit product format

005912170

Labeler code

0591

Product ID

0591-2170_70122f99-a4e4-4c32-8c5c-d843df4a974e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

valsartan

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Actavis Pharma, Inc.

Application

ANDA090642

Marketing category

ANDA

Marketing start

2015-01-05

Marketing end

2019-06-30

Substance

VALSARTAN

Active strength

320 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record