Sodium Acetate 00409-7299
Product NDC
00409-7299- Manufacturer
- Hospira, Inc.
- Dosage Form
- Injection, Solution, Concentrate
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- March 5, 2014
- Listing Expires
- December 31, 2027
- Application
- NDA018893
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sodium Acetate Anhydrous | 3.28 g/20mL |
Drug Class
Increased Large Intestinal Motility [PE]Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]Osmotic Activity [MoA]
Packaging Options(1)
25 VIAL, SINGLE-DOSE in 1 TRAY (0409-7299-25) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-7299-45)