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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 211641
Company: SUN PHARM
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
DEFERASIROX DEFERASIROX 90MG TABLET;ORAL Discontinued None No No
DEFERASIROX DEFERASIROX 360MG TABLET;ORAL Discontinued None No No
DEFERASIROX DEFERASIROX 180MG TABLET;ORAL Discontinued None No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
06/15/2020 ORIG-2 Approval STANDARD Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2020/211641Orig1Orig2s000TAltr.pdf
01/02/2020 ORIG-1 Approval STANDARD Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2020/211641Orig1Orig2s000TAltr.pdf
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
12/16/2024 SUPPL-2 Labeling-Package Insert, Labeling-Medication Guide

Label is not available on this site.

05/14/2020 SUPPL-1 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

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