NDC 43598-046
SUNITINIB MALATE
Sunitinib Malate
SUNITINIB MALATE is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Dr.reddys Laboratories Inc. The primary component is Sunitinib Malate.
| Product ID | 43598-046_64f82125-61a8-4e9c-2633-903ec6d5e9fc |
| NDC | 43598-046 |
| Product Type | Human Prescription Drug |
| Proprietary Name | SUNITINIB MALATE |
| Generic Name | Sunitinib Malate |
| Dosage Form | Capsule |
| Route of Administration | ORAL |
| Marketing Start Date | 2022-11-30 |
| Marketing Category | ANDA / |
| Application Number | ANDA215843 |
| Labeler Name | Dr.Reddys Laboratories Inc |
| Substance Name | SUNITINIB MALATE |
| Active Ingredient Strength | 25 mg/1 |
| Pharm Classes | Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |