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Business · 25/10/2019Updated: 10/17/2026 · 1 min read

FDA Withdraws Approval of Allergan's LO MINASTRIN FE Drug Application

Summary

The US Food and Drug Administration (FDA) has withdrawn approval of a new drug application for LO MINASTRIN FE, a birth control medication developed by Allergan Pharmaceuticals International, LTD, following a notification from the company that the product is no longer being marketed.

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

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