Benazepril Hydrochloride And Hydrochlorothiazide 62559-0417

Product NDC

62559-0417

Manufacturer: Ani Pharmaceuticals, Inc.
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: November 7, 2022
Listing Expires: December 31, 2026
Application: ANDA076342

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Active Ingredients

Ingredient	Strength
Benazepril Hydrochloride	20 mg/1
Hydrochlorothiazide	25 mg/1

Drug Class

Thiazide Diuretic [EPC]Angiotensin Converting Enzyme Inhibitor [EPC]Angiotensin-converting Enzyme Inhibitors [MoA]

Packaging Options(1)

62559-0417-01

100 TABLET in 1 BOTTLE (62559-417-01)

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