| NDC Code | 0121-1100-04 |
|---|
| Package Description | 5 mL in 1 BOTTLE (0121-1100-04) |
|---|
| Product NDC | 0121-1100 |
|---|
| 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 | 20260626 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA019157 |
|---|
| Manufacturer | PAI Holdings, LLC dba PAI Pharma |
|---|
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/5mL |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|