NDCFind

Benazepril Hydrochloride 68788-8877-01

Package NDC

68788-8877-01

Product NDC: 68788-8877

Manufacturer
Preferred Pharmaceuticals Inc.
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
May 19, 2025
Listing Expires
December 31, 2026
Application
ANDA078212
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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

68788-8877-01Selected

100 TABLET, FILM COATED in 1 BOTTLE (68788-8877-1)

Other packages for this product(3)

30 TABLET, FILM COATED in 1 BOTTLE (68788-8877-3)

60 TABLET, FILM COATED in 1 BOTTLE (68788-8877-6)

90 TABLET, FILM COATED in 1 BOTTLE (68788-8877-9)