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Benazepril Hydrochloride - 65862-117-01 - (Benazepril Hydrochloride)

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Drug Information of Benazepril Hydrochloride

Product NDC: 65862-117
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Benazepril Hydrochloride

Product NDC: 65862-117
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078212
Marketing Category: ANDA
Start Marketing Date: 20080522

Package Information of Benazepril Hydrochloride

Package NDC: 65862-117-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (65862-117-01)

NDC Information of Benazepril Hydrochloride

NDC Code 65862-117-01
Proprietary Name Benazepril Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (65862-117-01)
Product NDC 65862-117
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benazepril Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080522
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
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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