Benazepril Hydrochloride 65862-0117-01

Package NDC

65862-0117-01

Manufacturer: Aurobindo Pharma Limited
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 22, 2008
Application: ANDA078212

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Active Ingredients

Ingredient	Strength
Benazepril Hydrochloride	20 mg/1

Drug Class

Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]Decreased Blood Pressure [PE]

Selected Package

65862-0117-01Selected

100 TABLET, FILM COATED in 1 BOTTLE (65862-117-01)