Benazepril Hydrochloride And Hydrochlorothiazide 68462-0577

Product NDC

68462-0577

Manufacturer: Glenmark Pharmaceuticals Inc., Usa
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: April 4, 2014
Listing Expires: December 31, 2026
Application: ANDA076631

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Active Ingredients

Ingredient	Strength
Benazepril Hydrochloride	10 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)

68462-0577-01

100 TABLET, FILM COATED in 1 BOTTLE (68462-577-01)

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