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Benazepril Hydrochloride - 54458-956-10 - (Benazepril Hydrochloride)

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Drug Information of Benazepril Hydrochloride

Product NDC: 54458-956
Proprietary Name: Benazepril Hydrochloride
Non Proprietary Name: Benazepril Hydrochloride
Active Ingredient(s): 40    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: 54458-956
Labeler Name: International Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076402
Marketing Category: ANDA
Start Marketing Date: 20090301

Package Information of Benazepril Hydrochloride

Package NDC: 54458-956-10
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (54458-956-10)

NDC Information of Benazepril Hydrochloride

NDC Code 54458-956-10
Proprietary Name Benazepril Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (54458-956-10)
Product NDC 54458-956
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benazepril Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090301
Marketing Category Name ANDA
Labeler Name International Labs, Inc.
Substance Name BENAZEPRIL HYDROCHLORIDE
Strength Number 40
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