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Magnesium Sulfate
Magnesium Sulfate - 63323-064-20 - (MAGNESIUM SULFATE HEPTAHYDRATE)
Drug Information of Magnesium Sulfate
| Product NDC: | 63323-064 |
| Proprietary Name: | Magnesium Sulfate |
| Non Proprietary Name: | MAGNESIUM SULFATE HEPTAHYDRATE |
| Active Ingredient(s): | 500 mg/mL & nbsp; MAGNESIUM SULFATE HEPTAHYDRATE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Magnesium Sulfate
| Product NDC: | 63323-064 |
| Labeler Name: | Fresenius Kabi USA, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019316 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000808 |
Package Information of Magnesium Sulfate
| Package NDC: | 63323-064-20 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-064-20) > 20 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Magnesium Sulfate
| NDC Code | 63323-064-20 |
| Proprietary Name | Magnesium Sulfate |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-064-20) > 20 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 63323-064 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MAGNESIUM SULFATE HEPTAHYDRATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20000808 |
| Marketing Category Name | NDA |
| Labeler Name | Fresenius Kabi USA, LLC |
| Substance Name | MAGNESIUM SULFATE HEPTAHYDRATE |
| Strength Number | 500 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA] |
