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Benazepril Hydrochloride - 0904-6191-40 - (Benazepril Hydrochloride)

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Drug Information of Benazepril Hydrochloride

Product NDC: 0904-6191
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: 0904-6191
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076820
Marketing Category: ANDA
Start Marketing Date: 20100202

Package Information of Benazepril Hydrochloride

Package NDC: 0904-6191-40
Package Description: 500 TABLET in 1 BOTTLE (0904-6191-40)

NDC Information of Benazepril Hydrochloride

NDC Code 0904-6191-40
Proprietary Name Benazepril Hydrochloride
Package Description 500 TABLET in 1 BOTTLE (0904-6191-40)
Product NDC 0904-6191
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benazepril Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100202
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
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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