Benazepril Hydrochloride and Hydrochlorothiazide

Product NDC

0832-0484

11-digit product format

008320484

Labeler code

0832

Product ID

0832-0484_9b4ead99-96a1-4e09-a91b-c7d1cc27b5ab

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Benazepril Hydrochloride and Hydrochlorothiazide

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Upsher-Smith Laboratories, LLC

Application

ANDA076631

Marketing category

ANDA

Marketing start

2015-03-16

Marketing end

0000-00-00

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

2021-12-31

Current FDA listing

Historical FDA.report record