NDCFind

Hydrochlorothiazide 00172-2089-60

Package NDC

00172-2089-60

Product NDC: 00172-2089

Manufacturer
Teva Pharmaceuticals Usa, Inc.
Dosage Form
Tablet
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
January 7, 1980
Listing Expires
December 31, 2026
Application
ANDA083177
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Active Ingredients

IngredientStrength
Hydrochlorothiazide50 mg/1

Drug Class

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

Selected Package

00172-2089-60Selected

100 TABLET in 1 BOTTLE (0172-2089-60)

Other packages for this product(1)

1000 TABLET in 1 BOTTLE (0172-2089-80)