Chlorothiazide Sodium 47335-0330-40

Package NDC

47335-0330-40

Manufacturer: Sun Pharmaceutical Industries, Inc.
Dosage Form: Injection, Powder, Lyophilized, For Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: August 25, 2016
Listing Expires: December 31, 2026
Application: ANDA091546

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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

47335-0330-40Selected

1 VIAL, SINGLE-DOSE in 1 CARTON (47335-330-40) / 18 mL in 1 VIAL, SINGLE-DOSE