USFDA issues three observations for Lupin Pithampur facility

Written By :  Ruchika Sharma
Medically Reviewed By :  Dr. Kamal Kant Kohli
Published On 2024-09-28 06:45 GMT   |   Update On 2024-09-28 06:45 GMT

Mumbai: Lupin has announced that the United States Food and Drug Administration (USFDA) has issued three observations each on the API and Finished Product side of the Company's Pithampur facility.

The facility was inspection from  September 16 to September 27, 2024.

"We are addressing the observations comprehensively and will respond to the U.S. FDA within the stipulated timeframe," the Company stated in a BSE filing.

Lupin Limited is a global pharmaceutical leader headquartered in Mumbai, India, with products distributed in over 100 markets. Lupin specializes in pharmaceutical products, including branded and generic formulations, complex generics, biotechnology products, and active pharmaceutical ingredients. The company has a strong presence in India and the U.S. across multiple therapy areas, including respiratory, cardiovascular, anti-diabetic, anti-infective, gastrointestinal, central nervous system, and women’s health. Lupin has 15 state-of-the-art manufacturing sites and 7 research centers globally.

Read also: Lupin bags USFDA nod for Bumetanide Injection for edema treatment

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