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Benazepril Hydrochloride - 63629-1728-3 - (Benazepril Hydrochloride)

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Drug Information of Benazepril Hydrochloride

Product NDC: 63629-1728
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: 63629-1728
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076118
Marketing Category: ANDA
Start Marketing Date: 20100906

Package Information of Benazepril Hydrochloride

Package NDC: 63629-1728-3
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (63629-1728-3)

NDC Information of Benazepril Hydrochloride

NDC Code 63629-1728-3
Proprietary Name Benazepril Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (63629-1728-3)
Product NDC 63629-1728
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benazepril Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100906
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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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