Chlorothiazide Sodium 00517-1820-01

Package NDC

00517-1820-01

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

Ingredient	Strength
Chlorothiazide Sodium	500 mg/18mL

Drug Class

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

Selected Package

00517-1820-01Selected

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