| Product NDC: | 52533-107 |
| Proprietary Name: | Magnesium Sulfate |
| Non Proprietary Name: | Magnesium Sulfate |
| Active Ingredient(s): | 20 g/250mL & nbsp; Magnesium Sulfate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52533-107 |
| Labeler Name: | Cantrell Drug Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110725 |
| Package NDC: | 52533-107-38 |
| Package Description: | 250 mL in 1 BAG (52533-107-38) |
| NDC Code | 52533-107-38 |
| Proprietary Name | Magnesium Sulfate |
| Package Description | 250 mL in 1 BAG (52533-107-38) |
| Product NDC | 52533-107 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Magnesium Sulfate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110725 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cantrell Drug Company |
| Substance Name | MAGNESIUM SULFATE |
| Strength Number | 20 |
| Strength Unit | g/250mL |
| Pharmaceutical Classes | Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA] |