Hydrochlorothiazide 69315-0131-10

Package NDC

69315-0131-10

Manufacturer: Leading Pharma, Llc
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: April 1, 2016
Listing Expires: December 31, 2026
Application: ANDA040702

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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

69315-0131-10Selected

1000 TABLET in 1 BOTTLE, PLASTIC (69315-131-10)

Other packages for this product(2)

69315-0131-01

100 TABLET in 1 BOTTLE, PLASTIC (69315-131-01)

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69315-0131-50

5000 TABLET in 1 BOTTLE, PLASTIC (69315-131-50)

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