Amlodipine Besylate and Benazepril Hydrochloride

Product NDC

63629-7733

11-digit product format

636297733

Labeler code

63629

Product ID

63629-7733_61aeafd5-6206-4563-a129-fb13d60edd2f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine Besylate and Benazepril Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA077183

Marketing category

ANDA

Marketing start

2010-04-19

Marketing end

0000-00-00

Substance

AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE

Active strength

3 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

2021-12-31

Current FDA listing

Historical FDA.report record