NDC 63304-093
Sunitinib malate
Sunitinib Malate
Sunitinib malate is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Sun Pharmaceutical Industries Inc.. The primary component is Sunitinib Malate.
| Product ID | 63304-093_710053fe-e72c-4cbc-991e-fd19f6e93b44 |
| NDC | 63304-093 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Sunitinib malate |
| Generic Name | Sunitinib Malate |
| Dosage Form | Capsule |
| Route of Administration | ORAL |
| Marketing Start Date | 2019-12-25 |
| Marketing Category | ANDA / |
| Application Number | ANDA213914 |
| Labeler Name | Sun Pharmaceutical Industries Inc. |
| Substance Name | SUNITINIB MALATE |
| Active Ingredient Strength | 38 mg/1 |
| Pharm Classes | Protein Kinase Inhibitors [MoA],Kinase Inhibitor [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |