Amlodipine and Benazepril Hydrochloride

Product NDC

0591-3762

11-digit product format

005913762

Labeler code

0591

Product ID

0591-3762_d8c10de7-f915-4dc1-a167-6729f0015ee8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine and Benazepril Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Actavis Pharma, Inc.

Application

ANDA090364

Marketing category

ANDA

Marketing start

2011-07-05

Marketing end

2019-12-31

Substance

AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE

Active strength

10 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