NDCFind

Benazepril Hydrochloride 51655-0202-26

Package NDC

51655-0202-26

Product NDC: 51655-0202

Manufacturer
Northwind Health Company, Llc
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
March 15, 2023
Listing Expires
December 31, 2027
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

51655-0202-26Selected

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-202-26)