NDCFind

Benazepril Hydrochloride 68788-6889-06

Package NDC

68788-6889-06

Product NDC: 68788-6889

Manufacturer
Preferred Pharmaceuticals Inc.
Dosage Form
Tablet, Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
February 6, 2017
Listing Expires
December 31, 2027
Application
ANDA076118
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Active Ingredients

IngredientStrength
Benazepril Hydrochloride5 mg/1

Drug Class

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

Selected Package

68788-6889-06Selected

60 TABLET, COATED in 1 BOTTLE (68788-6889-6)

Other packages for this product(4)

100 TABLET, COATED in 1 BOTTLE (68788-6889-1)

30 TABLET, COATED in 1 BOTTLE (68788-6889-3)

120 TABLET, COATED in 1 BOTTLE (68788-6889-8)

90 TABLET, COATED in 1 BOTTLE (68788-6889-9)