BENAZEPRIL - 16590-259-60 - (BENAZEPRIL HYDROCHLORIDE)

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Drug Information of BENAZEPRIL

Product NDC: 16590-259
Proprietary Name: BENAZEPRIL
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

Product NDC: 16590-259
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076820
Marketing Category: ANDA
Start Marketing Date: 20100202

Package Information of BENAZEPRIL

Package NDC: 16590-259-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (16590-259-60)

NDC Information of BENAZEPRIL

NDC Code 16590-259-60
Proprietary Name BENAZEPRIL
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (16590-259-60)
Product NDC 16590-259
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 STAT RX USA LLC
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


General Information