Benazepril Hydrochloride And Hydrochlorothiazide 68462-0578

Product NDC

68462-0578

Manufacturer: Glenmark Pharmaceuticals Inc., Usa
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: February 11, 2004
Listing Expires: December 31, 2026
Application: ANDA076631

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Active Ingredients

Ingredient	Strength
Benazepril Hydrochloride	20 mg/1
Hydrochlorothiazide	12.5 mg/1

Drug Class

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

Packaging Options(1)

68462-0578-01

100 TABLET, FILM COATED in 1 BOTTLE (68462-578-01)

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