| NDC Code | 65162-667-90 |
|---|
| Package Description | 473 mL in 1 BOTTLE (65162-667-90) |
|---|
| Product NDC | 65162-667 |
|---|
| 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 | 20091201 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078345 |
|---|
| Manufacturer | Amneal Pharmaceuticals LLC |
|---|
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
|---|
| Strength | 15 |
|---|
| Strength Unit | mg/5mL |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|