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Abbreviated New Drug Application (ANDA): 209425
Company: APOTEX
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
CARFILZOMIB CARFILZOMIB 60MG/VIAL POWDER;INTRAVENOUS 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
03/16/2020 ORIG-1 Approval STANDARD Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2019/209425Orig1s000TAltr.pdf
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
11/24/2023 SUPPL-4 Labeling-Package Insert

Label is not available on this site.

11/24/2023 SUPPL-3 Labeling-Package Insert

Label is not available on this site.

11/24/2023 SUPPL-2 Labeling-Package Insert

Label is not available on this site.

11/24/2023 SUPPL-1 Labeling-Package Insert

Label is not available on this site.

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