NDCFind

Benazepril Hydrochloride 68071-3057-03

Package NDC

68071-3057-03

Product NDC: 68071-3057

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

IngredientStrength
Benazepril Hydrochloride10 mg/1

Drug Class

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

Selected Package

68071-3057-03Selected

30 TABLET, COATED in 1 BOTTLE (68071-3057-3)

Other packages for this product(3)

120 TABLET, COATED in 1 BOTTLE (68071-3057-2)

60 TABLET, COATED in 1 BOTTLE (68071-3057-6)

90 TABLET, COATED in 1 BOTTLE (68071-3057-9)