NDC Code | 70518-2459-0 |
Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (70518-2459-0) > 5 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 70518-2459 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Methylprednisolone Acetate |
Non-Proprietary Name | Methylprednisolone Acetate |
Dosage Form | INJECTION, SUSPENSION |
Usage | INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE |
Start Marketing Date | 20191202 |
Marketing Category Name | ANDA |
Application Number | ANDA040620 |
Manufacturer | REMEDYREPACK INC. |
Substance Name | METHYLPREDNISOLONE ACETATE |
Strength | 80 |
Strength Unit | mg/mL |
Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |