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Methylprednisolone Sodium Succinate
Methylprednisolone Sodium Succinate - 63323-265-30 - (METHYLPREDNISOLONE SODIUM SUCCINATE)
Drug Information of Methylprednisolone Sodium Succinate
| Product NDC: | 63323-265 |
| Proprietary Name: | Methylprednisolone Sodium Succinate |
| Non Proprietary Name: | METHYLPREDNISOLONE SODIUM SUCCINATE |
| Active Ingredient(s): | 1 g/16mL & nbsp; METHYLPREDNISOLONE SODIUM SUCCINATE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methylprednisolone Sodium Succinate
| Product NDC: | 63323-265 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040612 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20041130 |
Package Information of Methylprednisolone Sodium Succinate
| Package NDC: | 63323-265-30 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (63323-265-30) > 16 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Methylprednisolone Sodium Succinate
| NDC Code | 63323-265-30 |
| Proprietary Name | Methylprednisolone Sodium Succinate |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (63323-265-30) > 16 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 63323-265 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | METHYLPREDNISOLONE SODIUM SUCCINATE |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20041130 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | METHYLPREDNISOLONE SODIUM SUCCINATE |
| Strength Number | 1 |
| Strength Unit | g/16mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
