| 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] |