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Magnesium Sulfate
Magnesium Sulfate - 0517-2610-25 - (Magnesium Sulfate)
Drug Information of Magnesium Sulfate
| Product NDC: | 0517-2610 |
| Proprietary Name: | Magnesium Sulfate |
| Non Proprietary Name: | Magnesium Sulfate |
| Active Ingredient(s): | 500 mg/mL & nbsp; Magnesium Sulfate |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Magnesium Sulfate
| Product NDC: | 0517-2610 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19900930 |
Package Information of Magnesium Sulfate
| Package NDC: | 0517-2610-25 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-2610-25) > 10 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Magnesium Sulfate
| NDC Code | 0517-2610-25 |
| Proprietary Name | Magnesium Sulfate |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-2610-25) > 10 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0517-2610 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Magnesium Sulfate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19900930 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | American Regent, Inc. |
| Substance Name | MAGNESIUM SULFATE HEPTAHYDRATE |
| Strength Number | 500 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA] |
