NDCFind

Benazepril Hydrochloride 50090-3359-00

Package NDC

50090-3359-00

Product NDC: 50090-3359

Manufacturer
A-S Medication Solutions
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
May 22, 2008
Listing Expires
December 31, 2026
Application
ANDA078212
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Active Ingredients

IngredientStrength
Benazepril Hydrochloride40 mg/1

Drug Class

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

Selected Package

50090-3359-00Selected

30 TABLET, FILM COATED in 1 BOTTLE (50090-3359-0)

Other packages for this product(1)

90 TABLET, FILM COATED in 1 BOTTLE (50090-3359-1)