Benazepril Hydrochloride 23155-0752-01

Package NDC

23155-0752-01

Manufacturer: Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc.
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 20, 2022
Listing Expires: December 31, 2026
Application: ANDA076267

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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]

Selected Package

23155-0752-01Selected

100 TABLET in 1 BOTTLE (23155-752-01)

Other packages for this product(1)

23155-0752-05

500 TABLET in 1 BOTTLE (23155-752-05)

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