Sodium Chloride 00409-1141-02

Package NDC

00409-1141-02

Manufacturer: Hospira, Inc.
Dosage Form: Injection, Solution, Concentrate
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: April 30, 2005
Listing Expires: December 31, 2026
Application: NDA018897

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Active Ingredients

Ingredient	Strength
Sodium Chloride	234 mg/mL

Drug Class

Increased Large Intestinal Motility [PE]Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]Osmotic Activity [MoA]

Selected Package

00409-1141-02Selected

25 VIAL, PHARMACY BULK PACKAGE in 1 CASE (0409-1141-02) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (0409-1141-12)