NDCFind

Benazepril Hydrochloride 68788-9313-03

Package NDC

68788-9313-03

Product NDC: 68788-9313

Manufacturer
Preferred Pharmaceuticals, Inc.
Dosage Form
Tablet, Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
March 25, 2015
Listing Expires
December 31, 2027
Application
ANDA076118
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Active Ingredients

IngredientStrength
Benazepril Hydrochloride20 mg/1

Drug Class

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

Selected Package

68788-9313-03Selected

30 TABLET, COATED in 1 BOTTLE (68788-9313-3)

Other packages for this product(3)

100 TABLET, COATED in 1 BOTTLE (68788-9313-1)

60 TABLET, COATED in 1 BOTTLE (68788-9313-6)

90 TABLET, COATED in 1 BOTTLE (68788-9313-9)