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Medrol
Medrol - 0009-0176-01 - (METHYLPREDNISOLONE)
Drug Information of Medrol
| Product NDC: | 0009-0176 |
| Proprietary Name: | Medrol |
| Non Proprietary Name: | METHYLPREDNISOLONE |
| Active Ingredient(s): | 32 mg/1 & nbsp; METHYLPREDNISOLONE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Medrol
| Product NDC: | 0009-0176 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011153 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19571024 |
Package Information of Medrol
| Package NDC: | 0009-0176-01 |
| Package Description: | 25 TABLET in 1 BOTTLE (0009-0176-01) |
NDC Information of Medrol
| NDC Code | 0009-0176-01 |
| Proprietary Name | Medrol |
| Package Description | 25 TABLET in 1 BOTTLE (0009-0176-01) |
| Product NDC | 0009-0176 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | METHYLPREDNISOLONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19571024 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | METHYLPREDNISOLONE |
| Strength Number | 32 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
