Benazepril Hydrochloride

Product NDC

0378-0444

11-digit product format

003780444

Labeler code

0378

Product ID

0378-0444_bd3fb6bb-c35d-41c0-a34b-1cb5d7906c73

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

benazepril hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Pharmaceuticals Inc.

Application

ANDA076430

Marketing category

ANDA

Marketing start

2004-02-11

Marketing end

2020-07-31

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

0000-00-00

Current FDA listing

Historical FDA.report record