Amlodipine and Benazepril Hydrochloride

Product NDC

63629-7644

11-digit product format

636297644

Labeler code

63629

Product ID

63629-7644_5dffc23d-ccfe-4c63-a740-c225e2deb351

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine and Benazepril Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA077179

Marketing category

ANDA

Marketing start

2007-05-18

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