Prednisone is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Apotheca Inc.. The primary component is Prednisone.
| Product ID | 12634-188_280c9fe8-339a-177a-e054-00144ff88e88 |
| NDC | 12634-188 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Prednisone |
| Generic Name | Prednisone |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 1974-02-26 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA083677 |
| Labeler Name | Apotheca Inc. |
| Substance Name | PREDNISONE |
| Active Ingredient Strength | 20 mg/1 |
| Pharm Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 1974-02-26 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA083677 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-02-26 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA083677 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-02-26 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA083677 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-02-26 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA083677 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-02-26 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA083677 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-02-26 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA083677 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-02-26 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA083677 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-02-26 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA083677 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-02-26 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA083677 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-02-26 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA083677 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-02-26 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA083677 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-02-26 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA083677 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-02-26 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA083677 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-02-26 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA083677 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1974-02-26 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| PREDNISONE | 20 mg/1 |
| SPL SET ID: | 280c9fe8-3399-177a-e054-00144ff88e88 |
| 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 |