Product NDC: | 0389-0173 |
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, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0389-0173 |
Labeler Name: | The Torrance Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19900903 |
Package NDC: | 0389-0173-50 |
Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (0389-0173-50) > 50 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 0389-0173-50 |
Proprietary Name | Magnesium Chloride |
Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0389-0173-50) > 50 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 0389-0173 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Magnesium Chloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19900903 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | The Torrance Company |
Substance Name | MAGNESIUM CHLORIDE |
Strength Number | 200 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA] |