| NDC Code | 59212-702-48 |
|---|
| Package Description | 8 BLISTER PACK in 1 CARTON (59212-702-48) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (59212-702-06) |
|---|
| Product NDC | 59212-702 |
|---|
| 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 | Concordia Pharmaceuticals Inc. |
|---|
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE |
|---|
| Strength | 30 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|