BENAZEPRIL HYDROCHLORIDE

Product NDC

13811-629

11-digit product format

138110629

Labeler code

13811

Product ID

13811-629_df70c619-a81f-48c3-8ec7-0135dc1fb450

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benazepril hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Trigen Laboratories, Inc.

Application

ANDA076118

Marketing category

ANDA

Marketing start

2012-11-15

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record