Benazepril Hydrochloride

Product NDC

51079-146

11-digit product format

510790146

Labeler code

51079

Product ID

51079-146_7cd83fde-3bd9-21a8-e053-2a91aa0a0057

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

benazepril hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA076430

Marketing category

ANDA

Marketing start

2004-05-21

Marketing end

0000-00-00

Substance

BENAZEPRIL HYDROCHLORIDE

Active strength

20 mg/1

Pharmacologic classes

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