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Magnesium Chloride
Magnesium Chloride - 0517-5034-01 - (Magnesium Chloride)
Drug Information of Magnesium Chloride
| Product NDC: | 0517-5034 |
| 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) |
Labeler Information of Magnesium Chloride
| Product NDC: | 0517-5034 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19900930 |
Package Information of Magnesium Chloride
| Package NDC: | 0517-5034-01 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (0517-5034-01) > 50 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Magnesium Chloride
| NDC Code | 0517-5034-01 |
| Proprietary Name | Magnesium Chloride |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0517-5034-01) > 50 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 0517-5034 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Magnesium Chloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19900930 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | American Regent, Inc. |
| Substance Name | MAGNESIUM CHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
