Amlodipine and Benazepril Hydrochloride

Product NDC

68071-1878

11-digit product format

680711878

Labeler code

68071

Product ID

68071-1878_4b7d3378-86dc-0a5f-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine and Benazepril Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA077179

Marketing category

ANDA

Marketing start

2011-07-20

Marketing end

0000-00-00

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

2019-12-31

Current FDA listing

Historical FDA.report record