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Benazepril Hydrochloride - 55154-5673-0 - (Benazepril Hydrochloride)

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Drug Information of Benazepril Hydrochloride

Product NDC: 55154-5673
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: 55154-5673
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076430
Marketing Category: ANDA
Start Marketing Date: 20110816

Package Information of Benazepril Hydrochloride

Package NDC: 55154-5673-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5673-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Benazepril Hydrochloride

NDC Code 55154-5673-0
Proprietary Name Benazepril Hydrochloride
Package Description 10 BLISTER PACK in 1 BAG (55154-5673-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-5673
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benazepril Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110816
Marketing Category Name ANDA
Labeler Name Cardinal Health
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


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