Hydrochlorothiazide 42708-0079-30

Package NDC

42708-0079-30

Manufacturer: Qpharma, Inc.
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 15, 2008
Listing Expires: December 31, 2026
Application: ANDA040907

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Active Ingredients

Ingredient	Strength
Hydrochlorothiazide	25 mg/1

Drug Class

Thiazide Diuretic [EPC]Increased Diuresis [PE]Thiazide Diuretic [EPC]

Selected Package

42708-0079-30Selected

30 TABLET in 1 BOTTLE (42708-079-30)