Benazepril Hydrochloride

Product NDC

60760-081

11-digit product format

607600081

Labeler code

60760

Product ID

60760-081_7a01a929-9304-2bed-e053-2991aa0a1826

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benazepril Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

St. Mary's Medical Park Pharmacy

Application

ANDA076820

Marketing category

ANDA

Marketing start

2015-06-16

Marketing end

0000-00-00

Substance

BENAZEPRIL HYDROCHLORIDE

Active strength

10 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