Product NDC: | 52533-099 |
Proprietary Name: | Magnesium Sulfate |
Non Proprietary Name: | Magnesium Sulfate |
Active Ingredient(s): | 20 g/500mL & nbsp; Magnesium Sulfate |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52533-099 |
Labeler Name: | Cantrell Drug Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110221 |
Package NDC: | 52533-099-29 |
Package Description: | 500 mL in 1 BAG (52533-099-29) |
NDC Code | 52533-099-29 |
Proprietary Name | Magnesium Sulfate |
Package Description | 500 mL in 1 BAG (52533-099-29) |
Product NDC | 52533-099 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Magnesium Sulfate |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20110221 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Cantrell Drug Company |
Substance Name | MAGNESIUM SULFATE |
Strength Number | 20 |
Strength Unit | g/500mL |
Pharmaceutical Classes | Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA] |