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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 207586
Company: HIKMA
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
IMATINIB MESYLATE IMATINIB MESYLATE EQ 100MG BASE TABLET;ORAL Discontinued None No No
IMATINIB MESYLATE IMATINIB MESYLATE EQ 400MG BASE 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
07/13/2018 ORIG-1 Approval STANDARD

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
03/28/2024 SUPPL-5 Labeling-Package Insert

Label is not available on this site.

03/28/2024 SUPPL-4 Labeling-Package Insert

Label is not available on this site.

03/28/2024 SUPPL-3 Labeling-Package Insert

Label is not available on this site.

11/20/2018 SUPPL-2 Labeling-Package Insert

Label is not available on this site.

11/20/2018 SUPPL-1 Labeling-Container/Carton Labels

Label is not available on this site.

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