Benazepril Hydrochloride 84386-0102

Product NDC

84386-0102

Manufacturer: Aurobindo Pharma Limited
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 13, 2026
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)

84386-0102-01

100 TABLET, FILM COATED in 1 BOTTLE (84386-102-01)

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84386-0102-90

90 TABLET, FILM COATED in 1 BOTTLE (84386-102-90)

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