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Benazepril Hydrochloride - 21695-327-60 - (Benazepril Hydrochloride)

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Drug Information of Benazepril Hydrochloride

Product NDC: 21695-327
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: 21695-327
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076402
Marketing Category: ANDA
Start Marketing Date: 20040211

Package Information of Benazepril Hydrochloride

Package NDC: 21695-327-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (21695-327-60)

NDC Information of Benazepril Hydrochloride

NDC Code 21695-327-60
Proprietary Name Benazepril Hydrochloride
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (21695-327-60)
Product NDC 21695-327
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benazepril Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040211
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name BENAZEPRIL HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]

Complete Information of Benazepril Hydrochloride


General Information