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FDA Drug Approval, A213914, SUNITINIB MALATE
FDA Drug Approval, A213914, SUNITINIB MALATE
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ANDA: 213914
Company: SUN PHARM
Drug Name: SUNITINIB MALATE
Active Ingredients: SUNITINIB MALATE
Strength: EQ 50MG BASE
Dosage Form/Route: CAPSULE;ORAL
Action Date: 08/16/2021
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB
Company: SUN PHARM
Drug Name: SUNITINIB MALATE
Active Ingredients: SUNITINIB MALATE
Strength: EQ 50MG BASE
Dosage Form/Route: CAPSULE;ORAL
Action Date: 08/16/2021
Marketing Status: Prescription
Submission Classification: ORIG-1 TE Code: AB
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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