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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 214962
Company: CYCLE
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
TASCENSO ODT FINGOLIMOD LAURYL SULFATE EQ 0.25MG BASE TABLET, ORALLY DISINTEGRATING;ORAL Prescription None Yes No
TASCENSO ODT FINGOLIMOD LAURYL SULFATE EQ 0.5MG BASE TABLET, ORALLY DISINTEGRATING;ORAL Prescription None Yes Yes
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
12/23/2021 ORIG-2 Approval STANDARD Label (PDF)
Letter (PDF)
Review
https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/214962Orig2lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/214962Orig2s000ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2022/214962Orig2s000TOC.cfm
12/09/2022 ORIG-1 Approval Type 2 - New Active Ingredient STANDARD Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/214962s000lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2022/214962Orig1s000ltr.pdf
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
08/10/2023 SUPPL-1 Labeling-Package Insert Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/214962s001lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/214962Orig1s001ltr.pdf
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
08/10/2023 SUPPL-1 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/214962s001lbl.pdf
12/09/2022 ORIG-1 Approval Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/214962s000lbl.pdf
12/23/2021 ORIG-2 Approval Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2021/214962Orig2lbl.pdf
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