Everolimus is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Teva Pharmaceuticals Usa, Inc.. The primary component is Everolimus.
| Product ID | 0093-7766_06d60a83-bbb6-4fa7-a609-c520542907cc |
| NDC | 0093-7766 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Everolimus |
| Generic Name | Everolimus |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2020-06-10 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA210050 |
| Labeler Name | Teva Pharmaceuticals USA, Inc. |
| Substance Name | EVEROLIMUS |
| Active Ingredient Strength | 3 mg/1 |
| Pharm Classes | Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Decreased Immunologic Activity [PE], Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA], mTOR Inhibitor Immunosuppressant [EPC], mTOR Inhibitors [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |
| Marketing Start Date | 2020-06-10 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0054-0470 | Everolimus | Everolimus |
| 0054-0471 | Everolimus | Everolimus |
| 0054-0472 | Everolimus | Everolimus |
| 0054-0480 | Everolimus | Everolimus |
| 0054-0481 | Everolimus | Everolimus |
| 0054-0482 | Everolimus | Everolimus |
| 0054-0497 | Everolimus | Everolimus |
| 0054-0604 | Everolimus | Everolimus |
| 49884-119 | Everolimus | Everolimus |
| 49884-127 | Everolimus | Everolimus |
| 49884-125 | Everolimus | Everolimus |
| 0378-3098 | everolimus | everolimus |
| 0093-7766 | Everolimus | Everolimus |
| 0378-3097 | everolimus | everolimus |
| 0093-7767 | Everolimus | Everolimus |
| 0093-7768 | Everolimus | Everolimus |
| 0378-3096 | everolimus | everolimus |
| 0078-0414 | Zortress | everolimus |
| 0078-0415 | Zortress | everolimus |
| 0078-0417 | Zortress | everolimus |
| 0078-0422 | Zortress | everolimus |