NDCFind

Benazepril Hydrochloride 71335-1086-06

Package NDC

71335-1086-06

Product NDC: 71335-1086

Manufacturer
Bryant Ranch Prepack
Dosage Form
Tablet
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
February 2, 2010
Listing Expires
December 31, 2026
Application
ANDA076820
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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

71335-1086-06Selected

10 TABLET in 1 BOTTLE (71335-1086-6)

Other packages for this product(5)

30 TABLET in 1 BOTTLE (71335-1086-1)

60 TABLET in 1 BOTTLE (71335-1086-2)

100 TABLET in 1 BOTTLE (71335-1086-3)

90 TABLET in 1 BOTTLE (71335-1086-4)

14 TABLET in 1 BOTTLE (71335-1086-5)