Magnesium Sulfate 51662-1372
Product NDC
51662-1372- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Injection, Solution
- Route
- Intramuscular And Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- October 14, 2019
- Listing Expires
- December 31, 2026
- Application
- NDA019316
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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)
20 mL in 1 VIAL, SINGLE-DOSE (51662-1372-1)