benazepril hydrochloride and hydrochlorothiazide

Product NDC

60505-0263

11-digit product format

605050263

Labeler code

60505

Product ID

60505-0263_e62a2b3e-783f-1d7b-2e12-98b2ed97ddfa

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

benazepril hydrochloride and hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Apotex Corp.

Application

ANDA078794

Marketing category

ANDA

Marketing start

2014-08-21

Marketing end

2020-05-31

Substance

BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE

Active strength

20 mg/1; mg/1

Pharmacologic classes

Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record