Amlodipine Besylate and Benazepril Hydrochloride

Product NDC

63187-370

11-digit product format

631870370

Labeler code

63187

Product ID

63187-370_5a9f4cba-fb80-4001-811a-2fcff0408b16

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amlodipine Besylate and Benazepril Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Proficient Rx LP

Application

ANDA090364

Marketing category

ANDA

Marketing start

2011-07-05

Marketing end

0000-00-00

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

2020-12-31

Current FDA listing

Historical FDA.report record