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Benazepril Hydrochloride - 68788-9946-9 - (Benazepril Hydrochloride)

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Drug Information of Benazepril Hydrochloride

Product NDC: 68788-9946
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: 68788-9946
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076402
Marketing Category: ANDA
Start Marketing Date: 20120112

Package Information of Benazepril Hydrochloride

Package NDC: 68788-9946-9
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (68788-9946-9)

NDC Information of Benazepril Hydrochloride

NDC Code 68788-9946-9
Proprietary Name Benazepril Hydrochloride
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (68788-9946-9)
Product NDC 68788-9946
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benazepril Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120112
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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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