| NDC Code | 81033-021-54 |
|---|
| Package Description | 50 CUP, UNIT-DOSE in 1 CARTON (81033-021-54) / 5 mL in 1 CUP, UNIT-DOSE (81033-021-05) |
|---|
| Product NDC | 81033-021 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Prednisolone Sodium Phosphate |
|---|
| Non-Proprietary Name | Prednisolone Sodium Phosphate |
|---|
| Dosage Form | SOLUTION |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20231027 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203559 |
|---|
| Manufacturer | Kesin Pharma |
|---|
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
|---|
| Strength | 15 |
|---|
| Strength Unit | mg/5mL |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|