Benazepril Hydrochloride

Product NDC

68788-7248

11-digit product format

687887248

Labeler code

68788

Product ID

68788-7248_b4f0a7c3-1afe-42a5-a7c3-aa9512a8a6c0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benazepril Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA078212

Marketing category

ANDA

Marketing start

2018-08-27

Marketing end

0000-00-00

Substance

BENAZEPRIL HYDROCHLORIDE

Active strength

40 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

2020-12-31

Current FDA listing

Historical FDA.report record