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Methylprednisolone
Methylprednisolone - 50436-4037-1 - (Methylprednisolone)
Drug Information of Methylprednisolone
| Product NDC: | 50436-4037 |
| Proprietary Name: | Methylprednisolone |
| Non Proprietary Name: | Methylprednisolone |
| Active Ingredient(s): | 4 mg/1 & nbsp; Methylprednisolone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methylprednisolone
| Product NDC: | 50436-4037 |
| Labeler Name: | Unit Dose Services |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040189 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19971031 |
Package Information of Methylprednisolone
| Package NDC: | 50436-4037-1 |
| Package Description: | 21 TABLET in 1 BOTTLE (50436-4037-1) |
NDC Information of Methylprednisolone
| NDC Code | 50436-4037-1 |
| Proprietary Name | Methylprednisolone |
| Package Description | 21 TABLET in 1 BOTTLE (50436-4037-1) |
| Product NDC | 50436-4037 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methylprednisolone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19971031 |
| Marketing Category Name | ANDA |
| Labeler Name | Unit Dose Services |
| Substance Name | METHYLPREDNISOLONE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
