Sodium Chloride 00409-1141
Product NDC
00409-1141- 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]
Packaging Options(1)
25 VIAL, PHARMACY BULK PACKAGE in 1 CASE (0409-1141-02) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (0409-1141-12)