
Aurobindo Pharma Limited has informed the stock exchanges that the United States Food and Drug Administration (USFDA) has classified the Unit-I manufacturing facility of Eugia Pharma Specialities Limited, its wholly owned subsidiary, as “Official Action Indicated” (OAI).
The company stated that the development does not have any impact on its financial performance or operational activities.
The regulatory action relates to Unit-I, a formulations manufacturing facility operated by Eugia Pharma Specialities Limited at Kolthur Village, Shameerpet Mandal, Ranga Reddy district, Telangana. The USFDA conducted an inspection of the facility between February 16 and February 27, 2026.
The inspection concluded with four observations. Following its review, the USFDA determined the inspection classification of the facility as “Official Action Indicated” (OAI), according to the company’s disclosure.
Aurobindo Pharma stated that it received the communication from the USFDA on May 23, 2026. The company disclosed the development through an exchange filing dated May 24, 2026.
The regulatory classification applies specifically to the Eugia Pharma Specialities manufacturing facility that was inspected earlier this year. The company did not provide additional details regarding any further actions that may follow from the classification.
Read More: Aurobindo Pharma Share Price in Focus After USFDA Approval for Diabetes Drug!
As of 25 May 2026, at 9:21 AM, Aurobindo Pharma share price is trading at ₹1,451.80 per share, reflecting a decline of 0.80% from its previous closing price.
Aurobindo Pharma’s wholly owned subsidiary Eugia Pharma Specialities has received an OAI classification from the USFDA for its Unit-I formulations facility in Telangana following an inspection conducted in February 2026. The company has stated that the development does not affect its financial position or business operations.
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Published on: May 25, 2026, 9:41 AM IST

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