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Egis Pharmaceuticals Limited, et al.; Withdrawal of Approval of Three Abbreviated New Drug

The Food and Drug Administration (FDA or Agency) is withdrawing approval of three abbreviated new drug applications (ANDAs) from the holders of those ANDAs. The basis for the withdrawal is that the ANDA holders have repeatedly failed to file required annual reports for those ANDAs.

AgencyHealth and Human Services Department, Food and Drug Administration
Document typeNotice
Published2026-04-24
SummaryThe Food and Drug Administration (FDA or Agency) is withdrawing approval of three abbreviated new drug applications (ANDAs) from the holders of those ANDAs. The basis for the withdrawal is that the ANDA holders have repeatedly failed to file required annual reports for those ANDAs.
Document number2026-08020
Official recordhttps://www.federalregister.gov/documents/2026/04/24/2026-08020/egis-pharmaceuticals-limited-et-al-withdrawal-of-approval-of-three-abbreviated-new-drug-applications

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