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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 207231
Company: INVENTIA
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
ILOPERIDONE ILOPERIDONE 1MG TABLET;ORAL Discontinued None No No
ILOPERIDONE ILOPERIDONE 2MG TABLET;ORAL Discontinued None No No
ILOPERIDONE ILOPERIDONE 4MG TABLET;ORAL Discontinued None No No
ILOPERIDONE ILOPERIDONE 6MG TABLET;ORAL Discontinued None No No
ILOPERIDONE ILOPERIDONE 8MG TABLET;ORAL Discontinued None No No
ILOPERIDONE ILOPERIDONE 10MG TABLET;ORAL Discontinued None No No
ILOPERIDONE ILOPERIDONE 12MG 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
11/28/2016 ORIG-1 Approval STANDARD Letter (PDF)
Review (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/207231Orig1s000ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2023/207231Orig1s000.pdf
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
09/11/2020 SUPPL-2 Labeling-Package Insert

Label is not available on this site.

01/27/2020 SUPPL-1 Labeling-Package Insert, Labeling-Medication Guide

Label is not available on this site.

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