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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 022561
Company: EMD SERONO INC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
MAVENCLAD CLADRIBINE 10MG TABLET;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
03/29/2019 ORIG-1 Approval Type 3 - New Dosage Form STANDARD Label (PDF)
Letter (PDF)
Review
https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/022561s000lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/022561Orig1s000ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2019/022561Orig1s000TOC.cfm
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
05/10/2024 SUPPL-11 Labeling-Package Insert Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/022561s011lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2024/022561Orig1s011ltr.pdf
02/07/2024 SUPPL-9 Labeling-Package Insert Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/022561Orig1s009Corrected_lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2024/022561Orig1s009Corrected_ltr.pdf
12/06/2023 SUPPL-7 Labeling-Medication Guide, Labeling-Package Insert Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/022561s007lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2023/022561Orig1s007ltr.pdf
09/19/2022 SUPPL-6 Labeling-Package Insert Label (PDF)
Letter (PDF)
https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/022561s006lbl.pdf https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2022/022561Orig1s006ltr.pdf
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels,
Patient Package Insert
Note Url
05/10/2024 SUPPL-11 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/022561s011lbl.pdf
02/07/2024 SUPPL-9 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/022561Orig1s009Corrected_lbl.pdf
12/06/2023 SUPPL-7 Labeling-Medication Guide Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/022561s007lbl.pdf
12/06/2023 SUPPL-7 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/022561s007lbl.pdf
09/19/2022 SUPPL-6 Labeling-Package Insert Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2022/022561s006lbl.pdf
03/29/2019 ORIG-1 Approval Label (PDF) https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/022561s000lbl.pdf
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