Magnesium Sulfate 00409-2168
Product NDC
00409-2168- Manufacturer
- Hospira, Inc.
- Dosage Form
- Injection, Solution
- Route
- Intramuscular And Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- March 31, 2005
- Listing Expires
- December 31, 2027
- Application
- ANDA202411
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Magnesium Sulfate Heptahydrate | 500 mg/mL |
Drug Class
Calculi Dissolution Agent [EPC]Increased Large Intestinal Motility [PE]Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
Packaging Options(1)
25 VIAL, PLASTIC in 1 TRAY (0409-2168-77) / 20 mL in 1 VIAL, PLASTIC (0409-2168-17)