ANDA 211859, held by Zydus Pharms. Apremilast.
As of Nov 13, 2026, ANDA 211859 (Apremilast), held by Zydus Pharms, was not approved, with 0 approved supplements and 0 published complete response letters.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Feb 3, 2022 | Original application | Tentative approval | None posted |
| Apremilast10MG · tablet;oral | Apremilast | None (tentative approval) |
| Apremilast20MG · tablet;oral | Apremilast | None (tentative approval) |
| Apremilast30MG · tablet;oral | Apremilast | None (tentative approval) |
Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed daily; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters. Drugs@FDA and FDA complete response letters