Amlodipine and Benazepril Hydrochloride

Product NDC

0093-7371

11-digit product format

000937371

Labeler code

0093

Product ID

0093-7371_fae2ca85-de6d-424b-83f5-01680531f985

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine and Benazepril Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA077179

Marketing category

ANDA

Marketing start

2007-05-18

Marketing end

2020-04-30

Substance

AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE

Active strength

5 mg/1; mg/1

Pharmacologic classes

Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record