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Solu-Medrol
Solu-Medrol - 49349-840-41 - (Methylprednisolone Sodium Succinate)
Drug Information of Solu-Medrol
| Product NDC: | 49349-840 |
| Proprietary Name: | Solu-Medrol |
| Non Proprietary Name: | Methylprednisolone Sodium Succinate |
| Active Ingredient(s): | 125 mg/mL & nbsp; Methylprednisolone Sodium Succinate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Solu-Medrol
| Product NDC: | 49349-840 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011856 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20111219 |
Package Information of Solu-Medrol
| Package NDC: | 49349-840-41 |
| Package Description: | 1 mL in 1 VIAL (49349-840-41) |
NDC Information of Solu-Medrol
| NDC Code | 49349-840-41 |
| Proprietary Name | Solu-Medrol |
| Package Description | 1 mL in 1 VIAL (49349-840-41) |
| Product NDC | 49349-840 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methylprednisolone Sodium Succinate |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20111219 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | METHYLPREDNISOLONE SODIUM SUCCINATE |
| Strength Number | 125 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
