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Eugia Pharma Specialities’ Unit I formulation facility received a US FDA Warning Letter following its prior Official Action Indicated status. Existing US supplies are unaffected, and the unit contributes approximately 2% of group revenue. Context: crystallizes the previously pending regulatory overhang.
Aurobindo Pharma Gets FTC Approval for Lannett Acquisition, Closing This Month
Aurobindo Pharma's Unit-III Gets FDA OAI After 11 Inspection Observations