Product NDC: | 67457-134 |
Proprietary Name: | Magnesium Chloride |
Non Proprietary Name: | magnesium chloride |
Active Ingredient(s): | 200 mg/mL & nbsp; magnesium chloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67457-134 |
Labeler Name: | Mylan Institutional LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20130314 |
Package NDC: | 67457-134-50 |
Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (67457-134-50) > 50 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 67457-134-50 |
Proprietary Name | Magnesium Chloride |
Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (67457-134-50) > 50 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 67457-134 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | magnesium chloride |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20130314 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Mylan Institutional LLC |
Substance Name | MAGNESIUM CHLORIDE |
Strength Number | 200 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA] |