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 ID63304-093_710053fe-e72c-4cbc-991e-fd19f6e93b44
NDC63304-093
Product TypeHuman Prescription Drug
Proprietary NameSunitinib malate
Generic NameSunitinib Malate
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date2019-12-25
Marketing CategoryANDA /
Application NumberANDA213914
Labeler NameSun Pharmaceutical Industries Inc.
Substance NameSUNITINIB MALATE
Active Ingredient Strength38 mg/1
Pharm ClassesProtein Kinase Inhibitors [MoA],Kinase Inhibitor [EPC]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 63304-093-27

28 CAPSULE in 1 BOTTLE (63304-093-27)
Marketing Start Date2019-12-25
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Sunitinib malate" or generic name "Sunitinib Malate"

NDCBrand NameGeneric Name
0093-8199Sunitinib MalateSunitinib Malate
0093-8224Sunitinib MalateSunitinib Malate
0093-8229Sunitinib MalateSunitinib Malate
0093-8231Sunitinib MalateSunitinib Malate
0378-6678Sunitinib Malatesunitinib malate
0378-6679Sunitinib Malatesunitinib malate
0378-6680Sunitinib Malatesunitinib malate
0378-6681Sunitinib Malatesunitinib malate
16714-676Sunitinib malateSunitinib malate
16714-677Sunitinib malateSunitinib malate
0069-0550SUTENTSunitinib malate
0069-0770SUTENTSunitinib malate
0069-0830SUTENTSunitinib malate
0069-0980SUTENTSunitinib malate

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.