Benazepril Hydrochloride 68071-4722-09

Package NDC

68071-4722-09

Manufacturer: Nucare Pharmaceuticals,inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 22, 2008
Listing Expires: December 31, 2026
Application: ANDA078212

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Active Ingredients

Ingredient	Strength
Benazepril Hydrochloride	40 mg/1

Drug Class

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

Selected Package

68071-4722-09Selected

90 TABLET, FILM COATED in 1 BOTTLE (68071-4722-9)