Orapred ODT is a Oral Tablet, Orally Disintegrating in the Human Prescription Drug category. It is labeled and distributed by Concordia Pharmaceuticals Inc.. The primary component is Prednisolone Sodium Phosphate.
| Product ID | 59212-701_3ff164a5-ecb8-43d5-915b-ade2b585268a | 
| NDC | 59212-701 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | Orapred ODT | 
| Generic Name | Prednisolone Sodium Phosphate | 
| Dosage Form | Tablet, Orally Disintegrating | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2006-06-01 | 
| Marketing Category | NDA / NDA | 
| Application Number | NDA021959 | 
| Labeler Name | Concordia Pharmaceuticals Inc. | 
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE | 
| Active Ingredient Strength | 15 mg/1 | 
| Pharm Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2019-12-31 | 
| Marketing Start Date | 2020-06-30 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | NDA | 
| Application Number | NDA021959 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2006-06-01 | 
| Marketing Category | NDA | 
| Application Number | NDA021959 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2020-03-17 | 
| Marketing Category | NDA | 
| Application Number | NDA021959 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2006-06-01 | 
| Ingredient | Strength | 
|---|---|
| PREDNISOLONE SODIUM PHOSPHATE | 15 mg/1 | 
| SPL SET ID: | 1e379543-c4cf-4e72-953b-db15b7f0c2a1 | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 59212-701 | Orapred ODT | Orapred ODT | 
| 59212-702 | Orapred ODT | Orapred ODT | 
| 23594-510 | Millipred | PREDNISOLONE SODIUM PHOSPHATE | 
| 59212-700 | Orapred | prednisolone sodium phosphate | 
| 0121-0759 | Prednisolone Sodium Phosphate | Prednisolone Sodium Phosphate | 
| 0121-0773 | Prednisolone Sodium Phosphate | Prednisolone Sodium Phosphate | 
| 0121-0777 | Prednisolone Sodium Phosphate | Prednisolone Sodium Phosphate | 
| 0121-0902 | Prednisolone Sodium Phosphate | Prednisolone Sodium Phosphate | 
| 11695-1431 | Prednisolone Sodium Phosphate | PREDNISOLONE SODIUM PHOSPHATE | 
| 13925-166 | Prednisolone Sodium Phosphate | Prednisolone Sodium Phosphate | 
| 13985-025 | PREDNISOLONE SODIUM PHOSPHATE | PREDNISOLONE SODIUM PHOSPHATE | 
| 17856-0759 | Prednisolone Sodium Phosphate | Prednisolone Sodium Phosphate | 
| 24208-715 | PREDNISOLONE SODIUM PHOSPHATE | PREDNISOLONE SODIUM PHOSPHATE | 
| 42254-102 | Prednisolone Sodium Phosphate | Prednisolone Sodium Phosphate | 
| 42799-812 | Prednisolone Sodium Phosphate | Prednisolone Sodium Phosphate | 
| 42799-813 | Prednisolone Sodium Phosphate | Prednisolone Sodium Phosphate | 
| 50090-0955 | Prednisolone Sodium Phosphate | Prednisolone Sodium Phosphate | 
| 50090-1411 | Prednisolone Sodium Phosphate | Prednisolone Sodium Phosphate | 
| 50090-1582 | Prednisolone Sodium Phosphate | Prednisolone Sodium Phosphate | 
| 50383-040 | Prednisolone Sodium Phosphate | Prednisolone Sodium Phosphate | 
| 50436-0759 | Prednisolone Sodium Phosphate | Prednisolone Sodium Phosphate | 
| 0178-0582 | Prednisolone Sodium Phosphate Oral Solution | Prednisolone Sodium Phosphate | 
| 44523-182 | Prednisolone Sodium Phosphate Oral Solution | Prednisolone Sodium Phosphate | 
| 23594-915 | Veripred 20 | PREDNISOLONE SODIUM PHOSPHATE | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  ORAPRED  75284813  2185127 Live/Registered | CONCORDIA PHARMACEUTICALS INC. 1997-05-01 |