Methylprednisolone Sodium Succinate (Sagent Pharmaceuticals)
Welcome to the PulseAid listing for the Methylprednisolone Sodium Succinate drug offered from Sagent Pharmaceuticals. 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: | Sagent Pharmaceuticals |
| 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: | 2017-03-15 |
| END MARKETING DATE: | 0000-00-00 |
Methylprednisolone Sodium Succinate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Methylprednisolone Sodium Succinate from Sagent Pharmaceuticals |
| LABELER NAME: | Sagent Pharmaceuticals |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 40(mg/mL) |
| START MARKETING DATE: | 2017-03-15 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 25021-807_0bf9d0ea-b703-4eca-aab3-198f495ce63c |
| PRODUCT NDC: | 25021-807 |
| APPLICATION NUMBER: | ANDA040888 |
Other METHYLPREDNISOLONE SODIUM SUCCINATE Pharmaceutical Manufacturers / Labelers:
