Lupin rises after US FDA gives pharma firm EIR for its Aurangabad facility
Lupin said on Tuesday that it had received the Establishment Inspection Report (EIR) from the United States Food and Drug Administration (U.S. FDA) for its Aurangabad manufacturing facility. The inspection was conducted from March 6 to March 15, 2024. The U.S. FDA has determined that the inspection classification of the facility is Voluntary Action Indicated (VAI).
Lupin is large-cap pharmaceuticals company. Photo: File