Simplifying Global Compliance
FDA Issues Warning Letter to Lupin Pharmaceuticals
Drug GMP Report
Lupin products manufactured at its Mandideep, India, facility were cited for multiple GMP violations in a recent FDA warning letter.
|Correction: The July 2009 issue of Drug GMP Report incorrectly reported that products manufactured at Lupin Pharmaceuticals’ Mandideep facility in India were placed under an import alert after receiving a warning letter from the FDA. The facility did receive a warning letter for several GMP violations but no import alert was issued. FDAnews regrets the error.
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