Sodium Chloride 00409-6660-75

Package NDC

00409-6660-75

Manufacturer: Hospira, Inc.
Dosage Form: Injection, Solution, Concentrate
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: July 29, 2005
Listing Expires: December 31, 2027
Application: NDA018897

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Active Ingredients

Ingredient	Strength
Sodium Chloride	5.84 g/40mL

Drug Class

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

Selected Package

00409-6660-75Selected

25 VIAL in 1 TRAY (0409-6660-75) / 40 mL in 1 VIAL (0409-6660-01)