Benazepril Hydrochloride

Product NDC

43063-403

11-digit product format

430630403

Labeler code

43063

Product ID

43063-403_7c708638-6422-3a15-e053-2a91aa0a325e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benazepril Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA076118

Marketing category

ANDA

Marketing start

2010-09-06

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