NDC 43598-045
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 | 43598-045_64f82125-61a8-4e9c-2633-903ec6d5e9fc |
NDC | 43598-045 |
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 | 13 mg/1 |
Pharm Classes | Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |