Prednisone is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Northwind Pharmaceuticals. The primary component is Prednisone.
Product ID | 51655-320_abd6c038-2c14-4d9a-88a4-b823a8874b28 |
NDC | 51655-320 |
Product Type | Human Prescription Drug |
Proprietary Name | Prednisone |
Generic Name | Prednisone |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2014-05-01 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA088832 |
Labeler Name | Northwind Pharmaceuticals |
Substance Name | PREDNISONE |
Active Ingredient Strength | 20 mg/201 |
Pharm Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 2014-04-29 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA088832 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2014-04-29 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA088832 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2014-04-29 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA088832 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-01-22 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA088832 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2014-04-29 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA088832 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-01-22 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA088832 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2014-05-01 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
PREDNISONE | 20 mg/201 |
SPL SET ID: | 2a994060-a358-4835-892b-0eb1f0806eb0 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0054-0017 | PredniSONE | PredniSONE |
0054-0018 | PredniSONE | PredniSONE |
0054-0019 | PredniSONE | PredniSONE |
0054-3722 | PredniSONE | PredniSONE |
0054-4728 | PredniSONE | PredniSONE |
0054-4741 | PredniSONE | PredniSONE |
68071-1777 | Prednisone | Prednisone |
68071-1779 | Prednisone | Prednisone |
68071-3143 | Prednisone | Prednisone |
68071-4319 | Prednisone | Prednisone |
68071-4546 | Prednisone | Prednisone |
68071-4685 | Prednisone | Prednisone |
68071-4691 | Prednisone | Prednisone |
68071-4491 | Prednisone | Prednisone |
68151-0820 | PredniSONE | PredniSONE |
0440-8167 | Prednisone | Prednisone |
0440-8165 | Prednisone | Prednisone |
0463-6155 | PredniSONE | PredniSONE |
68258-3013 | Prednisone | Prednisone |
0463-6141 | PredniSONE | PredniSONE |
68387-240 | Prednisone | Prednisone |
68387-241 | Prednisone | Prednisone |
68788-6440 | Prednisone | Prednisone |
68788-6414 | Prednisone | Prednisone |
68788-7281 | Prednisone | Prednisone |
68788-7372 | Prednisone | Prednisone |
68788-9309 | Prednisone | Prednisone |
68788-9178 | Prednisone | Prednisone |
68788-9551 | Prednisone | Prednisone |
0054-4742 | PredniSONE | PredniSONE |
0054-8739 | PredniSONE | PredniSONE |
0054-8724 | PredniSONE | PredniSONE |
0054-8740 | PredniSONE | PredniSONE |
70518-0305 | Prednisone | Prednisone |
70518-0307 | Prednisone | Prednisone |
70518-0205 | Prednisone | Prednisone |
70518-0306 | PredniSONE | PredniSONE |
70518-0242 | Prednisone | Prednisone |
70518-0073 | Prednisone | Prednisone |
70518-0473 | Prednisone | Prednisone |
70518-0632 | Prednisone | Prednisone |
70518-1116 | PredniSONE | PredniSONE |
70518-1167 | Prednisone | Prednisone |
70518-0948 | Prednisone | Prednisone |
70518-0800 | Prednisone | Prednisone |
70518-1105 | PredniSONE | PredniSONE |
70518-1119 | Prednisone | Prednisone |
70518-1120 | Prednisone | Prednisone |
0591-5442 | Prednisone | Prednisone |
70518-1854 | Prednisone | Prednisone |