NDC Code | 70121-1000-5 |
Package Description | 25 VIAL in 1 CARTON (70121-1000-5) / 1 mL in 1 VIAL (70121-1000-1) |
Product NDC | 70121-1000 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Methylprednisolone Sodium Succinate |
Non-Proprietary Name | Methylprednisolone |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20161111 |
Marketing Category Name | ANDA |
Application Number | ANDA207549 |
Manufacturer | Amneal Pharmaceuticals LLC |
Substance Name | METHYLPREDNISOLONE SODIUM SUCCINATE |
Strength | 40 |
Strength Unit | mg/mL |
Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |