Benazepril Hydrochloride 68071-1769

Product NDC

68071-1769

Manufacturer: Nucare Pharmaceuticals,inc.
Dosage Form: Tablet, Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 1, 2014
Listing Expires: December 31, 2026
Application: ANDA076118

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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]

Packaging Options(1)

68071-1769-01

100 TABLET, COATED in 1 BOTTLE (68071-1769-1)

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