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SOLU-MEDROL
SOLU-MEDROL - 0009-0039-32 - (methylprednisolone sodium succinate)
Drug Information of SOLU-MEDROL
| Product NDC: | 0009-0039 |
| Proprietary Name: | SOLU-MEDROL |
| Non Proprietary Name: | methylprednisolone sodium succinate |
| Active Ingredient(s): | 40 mg/mL & nbsp; methylprednisolone sodium succinate |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SOLU-MEDROL
| Product NDC: | 0009-0039 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011856 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19590402 |
Package Information of SOLU-MEDROL
| Package NDC: | 0009-0039-32 |
| Package Description: | 25 VIAL, PATENT DELIVERY SYSTEM in 1 PACKAGE (0009-0039-32) > 1 mL in 1 VIAL, PATENT DELIVERY SYSTEM (0009-0039-33) |
NDC Information of SOLU-MEDROL
| NDC Code | 0009-0039-32 |
| Proprietary Name | SOLU-MEDROL |
| Package Description | 25 VIAL, PATENT DELIVERY SYSTEM in 1 PACKAGE (0009-0039-32) > 1 mL in 1 VIAL, PATENT DELIVERY SYSTEM (0009-0039-33) |
| Product NDC | 0009-0039 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methylprednisolone sodium succinate |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19590402 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | METHYLPREDNISOLONE SODIUM SUCCINATE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
