Product ID | 0338-1709_1bbaebd0-3f4c-467d-96fd-69cfad5a3fd3 |
NDC | 0338-1709 |
Product Type | Human Prescription Drug |
Proprietary Name | MAGNESIUM SULFATE IN DEXTROSE |
Generic Name | Magnesium Sulfate In Dextrose |
Dosage Form | Injection, Solution |
Route of Administration | INTRAVENOUS |
Marketing Start Date | 2020-08-11 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA211965 |
Labeler Name | Baxter Healthcare Corporation |
Substance Name | MAGNESIUM SULFATE HEPTAHYDRATE |
Active Ingredient Strength | 10 mg/mL |
Pharm Classes | Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |