Product NDC: | 0409-6727 |
Proprietary Name: | Magnesium Sulfate in Dextrose |
Non Proprietary Name: | MAGNESIUM SULFATE HEPTAHYDRATE |
Active Ingredient(s): | 10 mg/mL & nbsp; MAGNESIUM SULFATE HEPTAHYDRATE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-6727 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020488 |
Marketing Category: | NDA |
Start Marketing Date: | 19950711 |
Package NDC: | 0409-6727-23 |
Package Description: | 24 POUCH in 1 CASE (0409-6727-23) > 1 BAG in 1 POUCH > 100 mL in 1 BAG |
NDC Code | 0409-6727-23 |
Proprietary Name | Magnesium Sulfate in Dextrose |
Package Description | 24 POUCH in 1 CASE (0409-6727-23) > 1 BAG in 1 POUCH > 100 mL in 1 BAG |
Product NDC | 0409-6727 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | MAGNESIUM SULFATE HEPTAHYDRATE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19950711 |
Marketing Category Name | NDA |
Labeler Name | Hospira, Inc. |
Substance Name | MAGNESIUM SULFATE HEPTAHYDRATE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA] |