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Benazepril Hydrochloride - 42291-162-18 - (Benazepril Hydrochloride)

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Drug Information of Benazepril Hydrochloride

Product NDC: 42291-162
Proprietary Name: Benazepril Hydrochloride
Non Proprietary Name: Benazepril Hydrochloride
Active Ingredient(s): 20    mg/1 & nbsp;   Benazepril Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Benazepril Hydrochloride

Product NDC: 42291-162
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076820
Marketing Category: ANDA
Start Marketing Date: 20090729

Package Information of Benazepril Hydrochloride

Package NDC: 42291-162-18
Package Description: 180 TABLET in 1 BOTTLE (42291-162-18)

NDC Information of Benazepril Hydrochloride

NDC Code 42291-162-18
Proprietary Name Benazepril Hydrochloride
Package Description 180 TABLET in 1 BOTTLE (42291-162-18)
Product NDC 42291-162
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benazepril Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090729
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
Substance Name BENAZEPRIL HYDROCHLORIDE
Strength Number 20
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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