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 | 59212-702_3ff164a5-ecb8-43d5-915b-ade2b585268a |
NDC | 59212-702 |
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 | 30 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 |
Marketing Start Date | 2020-03-17 |
Marketing Category | NDA |
Application Number | NDA021959 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-06-01 |
Ingredient | Strength |
---|---|
PREDNISOLONE SODIUM PHOSPHATE | 30 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 |