Amlodipine and Valsartan

Product NDC

0093-7690

11-digit product format

000937690

Labeler code

0093

Product ID

0093-7690_7daefded-c14c-491b-bcd7-78de21562ae2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine and Valsartan

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA091235

Marketing category

ANDA

Marketing start

2015-03-30

Marketing end

2019-04-30

Substance

AMLODIPINE BESYLATE; VALSARTAN

Active strength

5 mg/1; mg/1

Pharmacologic classes

Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],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