U.S. Food and Drug Administration (USFDA) has concluded an inspection at Lupin’s Nagpur Injectable facility. USFDA has conducted the said inspection from September 08 to September 16, 2025. The inspection closed with six observations.
The company will address the observations and respond to the U.S. FDA within the stipulated timeframe. The company is committed to be compliant with CGMP quality standards across all its facilities.
Lupin is an innovation led transnational pharmaceutical company producing, developing and marketing a wide range of branded and generic formulations, biotechnology products and active pharmaceutical ingredients (APIs) globally.
