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Solu-Medrol
Solu-Medrol - 0009-0796-01 - (methylprednisolone sodium succinate)
Drug Information of Solu-Medrol
| Product NDC: | 0009-0796 |
| Proprietary Name: | Solu-Medrol |
| Non Proprietary Name: | methylprednisolone sodium succinate |
| Active Ingredient(s): | & nbsp; methylprednisolone sodium succinate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Solu-Medrol
| Product NDC: | 0009-0796 |
| 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: | 0009-0796-01 |
| Package Description: | 1 KIT in 1 CARTON (0009-0796-01) * 30.6 mL in 1 VIAL * 30.6 mL in 1 VIAL |
NDC Information of Solu-Medrol
| NDC Code | 0009-0796-01 |
| Proprietary Name | Solu-Medrol |
| Package Description | 1 KIT in 1 CARTON (0009-0796-01) * 30.6 mL in 1 VIAL * 30.6 mL in 1 VIAL |
| Product NDC | 0009-0796 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methylprednisolone sodium succinate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19590402 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
