Granules India’s Hyderabad Unit Gets ‘Official Action Indicated’ Classification From USFDA
The OAI classification from the USFDA indicates that the facility is in 'an unacceptable state of compliance'.
Granules India Ltd. on Tuesday said that the US Food and Drug Administration has issued 'official action indicated' classification for its Hyderabad-based facility.
The USFDA's OAI classification indicates that a facility is in "an unacceptable state of compliance", according to the US drug regulator's website.
Earlier, in September, the company had informed stock exchanges that the USFDA had completed its inspection at the Hyderabad plant with six observations. This inspection by the USFDA was conducted between Aug. 26 and Sept. 6.
In Tuesday's exchange filing, the company also said that in addition to responding to all the observations issued by the USFDA, it has voluntarily undertaken a comprehensive evaluation of the facility for further enhancements that lead to improvement of the facility. This activity is undertaken in consultation with external subject matter experts.
The Hyderabad-based pharmaceutical major reiterated that it will work with the USFDA to comply with its expectations.
In November, in an interview with NDTV Profit, Granules India Chairman and Managing Director Krishna Prasad Chigurupati had said that the company expects its financials to return to normalcy only after clarity over the observations made by the USFDA regarding its facility in Hyderabad.
In the quarter ended September, the company had reported a 19% year-on-year plunge in its revenue to Rs 966 crore from Rs 1,189 crore in the same quarter of the last fiscal. The net profit slipped 5% to Rs 97 crore from Rs 110 crore in the year-ago period.
Shares of Granules India closed 10.12% lower at Rs 534.45 apiece on the BSE, compared to a 0.74% advance in the benchmark Sensex.
