Hydrochlorothiazide 72789-0512-30

Package NDC

72789-0512-30

Manufacturer: Pd-Rx Pharmaceuticals, Inc.
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 12, 1973
Listing Expires: December 31, 2026
Application: ANDA083177

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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

72789-0512-30Selected

30 TABLET in 1 BOTTLE, PLASTIC (72789-512-30)

Other packages for this product(2)

72789-0512-60

60 TABLET in 1 BOTTLE, PLASTIC (72789-512-60)

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72789-0512-90

90 TABLET in 1 BOTTLE, PLASTIC (72789-512-90)

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