Benazepril Hydrochloride 51655-0617

Product NDC

51655-0617

Manufacturer: Northwind Health Company, Llc
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: September 6, 2022
Listing Expires: December 31, 2027
Application: ANDA078212

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Active Ingredients

Ingredient	Strength
Benazepril Hydrochloride	40 mg/1

Drug Class

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

Packaging Options(2)

51655-0617-26

90 TABLET, FILM COATED in 1 BOTTLE (51655-617-26)

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51655-0617-52

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-617-52)

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