Strength
9 mg/mL
Manufacturer
Fresenius Kabi USA, LLCNDC
63323018610
Classification
Generic
Dosage Form
INJECTION
Route
INTRAVENOUS
Last Updated
4/22/2026
Active Ingredients
SODIUM CHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA088912On Market Since
8/10/2000
Pharmacological Classes
Increased Large Intestinal Motility
Inhibition Large Intestine Fluid/Electrolyte Absorption
Osmotic Activity
Osmotic Laxative
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