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Benazepril Hydrochloride - 54868-5079-2 - (Benazepril Hydrochloride)

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Drug Information of Benazepril Hydrochloride

Product NDC: 54868-5079
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Benazepril Hydrochloride

Product NDC: 54868-5079
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076211
Marketing Category: ANDA
Start Marketing Date: 20040825

Package Information of Benazepril Hydrochloride

Package NDC: 54868-5079-2
Package Description: 90 TABLET, COATED in 1 BOTTLE (54868-5079-2)

NDC Information of Benazepril Hydrochloride

NDC Code 54868-5079-2
Proprietary Name Benazepril Hydrochloride
Package Description 90 TABLET, COATED in 1 BOTTLE (54868-5079-2)
Product NDC 54868-5079
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benazepril Hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20040825
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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