Lupin has received a communication from the USFDA classifying the inspection conducted at its Toropur manufacturing (API) facility between September 16-20, 2019, as Official Action Indicated (OAI). The inspection at the Toropur facility had closed with three observations. The company is in the process of sending further updates of its corrective actions to the USFDA and is hopeful of a positive outcome.
Lupin is an innovation led transnational pharmaceutical company developing and delivering a wide range of branded & generic formulations, biotechnology products and APIs globally.