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MethylpredniSOLONE
MethylpredniSOLONE - 51991-188-31 - (METHYLPREDNISOLONE)
Drug Information of MethylpredniSOLONE
| Product NDC: | 51991-188 |
| 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: | 51991-188 |
| Labeler Name: | Breckenridge Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040189 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20031107 |
Package Information of MethylpredniSOLONE
| Package NDC: | 51991-188-31 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (51991-188-31) > 21 TABLET in 1 BLISTER PACK |
NDC Information of MethylpredniSOLONE
| NDC Code | 51991-188-31 |
| Proprietary Name | MethylpredniSOLONE |
| Package Description | 1 BLISTER PACK in 1 CARTON (51991-188-31) > 21 TABLET in 1 BLISTER PACK |
| Product NDC | 51991-188 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | METHYLPREDNISOLONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20031107 |
| Marketing Category Name | ANDA |
| Labeler Name | Breckenridge Pharmaceutical, Inc. |
| Substance Name | METHYLPREDNISOLONE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
