Benazepril Hydrochloride

Product NDC

43063-787

11-digit product format

430630787

Labeler code

43063

Product ID

43063-787_77e6b501-8c89-ffae-e053-2991aa0a24a9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benazepril Hydrochloride

Dosage form

TABLET, COATED

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA076118

Marketing category

ANDA

Marketing start

2014-01-01

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

2019-12-31

Current FDA listing

Historical FDA.report record