Business · 02/07/2020Updated: 10/17/2026 · 1 min read

Teva Withdraws FDA Approval for ZECUITY Sumatriptan Iontophoretic Transdermal System

Summary

The FDA is withdrawing approval of a new drug application for ZECUITY, a sumatriptan iontophoretic transdermal system, submitted by Teva Branded Pharmaceutical Products R&D, Inc., after Teva requested withdrawal and waived its right to a hearing.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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