NDCFind

Chlorothiazide Sodium 00517-1820

Product NDC

00517-1820
Manufacturer
American Regent, Inc.
Dosage Form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Product Type
Human Prescription Drug
Marketing Start
April 1, 2015
Listing Expires
December 31, 2026
Application
ANDA202561
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Active Ingredients

IngredientStrength
Chlorothiazide Sodium500 mg/18mL

Drug Class

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

Packaging Options(1)

1 VIAL in 1 CARTON (0517-1820-01) / 18 mL in 1 VIAL