Hydrochlorothiazide 72789-0303-01

Package NDC

72789-0303-01

Manufacturer: Pd-Rx Pharmaceuticals, 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	50 mg/1

Drug Class

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

Selected Package

72789-0303-01Selected

100 TABLET in 1 BOTTLE, PLASTIC (72789-303-01)