Methylprednisolone Sodium Succinate (AuroMedics Pharma LLC)
Welcome to the PulseAid listing for the Methylprednisolone Sodium Succinate drug offered from AuroMedics Pharma LLC. This Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | AuroMedics Pharma LLC |
| NON-PROPRIETARY NAME: | Methylprednisolone Sodium Succinate |
| SUBSTANCE NAME: | METHYLPREDNISOLONE SODIUM SUCCINATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
| ROUTE: | INTRAMUSCULAR; INTRAVENOUS |
| DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2015-12-15 |
| END MARKETING DATE: | 0000-00-00 |
Methylprednisolone Sodium Succinate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Methylprednisolone Sodium Succinate from AuroMedics Pharma LLC |
| LABELER NAME: | AuroMedics Pharma LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 40(mg/1) |
| START MARKETING DATE: | 2015-12-15 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 55150-262_875c7844-2607-4edb-ae16-345f348a9536 |
| PRODUCT NDC: | 55150-262 |
| APPLICATION NUMBER: | ANDA207667 |
Other METHYLPREDNISOLONE SODIUM SUCCINATE Pharmaceutical Manufacturers / Labelers:
