| NDC Code | 0121-0773-08 |
|---|
| Package Description | 237 mL in 1 BOTTLE (0121-0773-08) |
|---|
| Product NDC | 0121-0773 |
|---|
| 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 | 20170131 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078465 |
|---|
| Manufacturer | Pharmaceutical Associates, Inc. |
|---|
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/5mL |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|