| NDC Code | 59630-700-48 |
|---|
| Package Description | 8 BLISTER PACK in 1 CARTON (59630-700-48) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
|---|
| Product NDC | 59630-700 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Orapred |
|---|
| Proprietary Name Suffix | Odt |
|---|
| Non-Proprietary Name | Prednisolone Sodium Phosphate |
|---|
| Dosage Form | TABLET, ORALLY DISINTEGRATING |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20060601 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA021959 |
|---|
| Manufacturer | Shionogi Inc. |
|---|
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
|---|