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Benazepril Hydrochloride - 0093-5125-05 - (Benazepril Hydrochloride)

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Drug Information of Benazepril Hydrochloride

Product NDC: 0093-5125
Proprietary Name: Benazepril Hydrochloride
Non Proprietary Name: Benazepril Hydrochloride
Active Ingredient(s): 10    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: 0093-5125
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076211
Marketing Category: ANDA
Start Marketing Date: 20040211

Package Information of Benazepril Hydrochloride

Package NDC: 0093-5125-05
Package Description: 500 TABLET, COATED in 1 BOTTLE (0093-5125-05)

NDC Information of Benazepril Hydrochloride

NDC Code 0093-5125-05
Proprietary Name Benazepril Hydrochloride
Package Description 500 TABLET, COATED in 1 BOTTLE (0093-5125-05)
Product NDC 0093-5125
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benazepril Hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20040211
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name BENAZEPRIL HYDROCHLORIDE
Strength Number 10
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


General Information