| NDC Code | 17856-0759-7 |
|---|
| Package Description | 1 BOX, UNIT-DOSE in 1 CUP, UNIT-DOSE (17856-0759-7) / 72 CUP in 1 BOX, UNIT-DOSE / 5 mL in 1 CUP (17856-0759-5) |
|---|
| Product NDC | 17856-0759 |
|---|
| 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 | 20050425 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076913 |
|---|
| Manufacturer | ATLANTIC BIOLOGICALS CORP. |
|---|
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
|---|
| Strength | 15 |
|---|
| Strength Unit | mg/5mL |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|