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MethylPREDNISolone
MethylPREDNISolone - 35356-763-21 - (methylprednisolone)
Drug Information of MethylPREDNISolone
| Product NDC: | 35356-763 |
| 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: | 35356-763 |
| Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040183 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19981222 |
Package Information of MethylPREDNISolone
| Package NDC: | 35356-763-21 |
| Package Description: | 1 DOSE PACK in 1 CARTON (35356-763-21) > 21 TABLET in 1 DOSE PACK |
NDC Information of MethylPREDNISolone
| NDC Code | 35356-763-21 |
| Proprietary Name | MethylPREDNISolone |
| Package Description | 1 DOSE PACK in 1 CARTON (35356-763-21) > 21 TABLET in 1 DOSE PACK |
| Product NDC | 35356-763 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methylprednisolone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19981222 |
| Marketing Category Name | ANDA |
| Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
| Substance Name | METHYLPREDNISOLONE |
| Strength Number | 4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
