Natco Pharma gets EIR from FDA for Hyd facility

New Delhi: Drug firm Natco Pharma on Tuesday said it has received establishment inspection report (EIR) from the US health regulator for its facility near Hyderabad.

In a BSE filing, Natco Pharma announced "successful closure of inspection" with the receipt of an establishment inspection report (EIR) from the US Food and Drug Administration (USFDA) for the inspection conducted at its active pharmaceutical ingredient (API) facility in Mekaguda Village, near Hyderabad, India.

The plant was inspected during the period August 5-9, 2019, it added. The USFDA gives EIR on closure of inspection of an establishment that is the subject of an FDA or FDA-contracted inspection.