Home > National Drug Code (NDC) > BENAZEPRIL HYDROCHLORIDE

BENAZEPRIL HYDROCHLORIDE - 13811-628-10 - (Benazepril hydrochloride)

Alphabetical Index


Drug Information of BENAZEPRIL HYDROCHLORIDE

Product NDC: 13811-628
Proprietary Name: BENAZEPRIL HYDROCHLORIDE
Non Proprietary Name: Benazepril hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Benazepril hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of BENAZEPRIL HYDROCHLORIDE

Product NDC: 13811-628
Labeler Name: Trigen Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076118
Marketing Category: ANDA
Start Marketing Date: 20121115

Package Information of BENAZEPRIL HYDROCHLORIDE

Package NDC: 13811-628-10
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (13811-628-10)

NDC Information of BENAZEPRIL HYDROCHLORIDE

NDC Code 13811-628-10
Proprietary Name BENAZEPRIL HYDROCHLORIDE
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (13811-628-10)
Product NDC 13811-628
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benazepril hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121115
Marketing Category Name ANDA
Labeler Name Trigen Laboratories, Inc.
Substance Name BENAZEPRIL HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]

Complete Information of BENAZEPRIL HYDROCHLORIDE


General Information