Sodium Chloride 00641-0497-25

Package NDC

00641-0497-25

Manufacturer: Hikma Pharmaceuticals Usa Inc.
Dosage Form: Injection
Route: Intramuscular, Intravenous, And Subcutaneous
Product Type: Human Prescription Drug
Marketing Start: September 24, 2013
Listing Expires: December 31, 2026
Application: ANDA201833

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Active Ingredients

Ingredient	Strength
Sodium Chloride	9 mg/mL

Drug Class

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

Selected Package

00641-0497-25Selected

25 VIAL in 1 CARTON (0641-0497-25) / 2 mL in 1 VIAL (0641-0497-17)