Benazepril Hydrochloride 70518-4633-00

Package NDC

70518-4633-00

Manufacturer: Remedyrepack Inc.
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: April 25, 2026
Listing Expires: December 31, 2027
Application: ANDA076267

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Active Ingredients

Ingredient	Strength
Benazepril Hydrochloride	20 mg/1

Drug Class

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

Selected Package

70518-4633-00Selected

90 TABLET in 1 BOTTLE, PLASTIC (70518-4633-0)