The agreement is for delivery over the two months following an
emergency use authorization if granted by U.S. regulators. The U.S.
government also has the provision to purchase up to an additional
650,000 vials through June 30, 2021, the company said.
The company submitted a request to the U.S. Food and Drug
Administration in October for emergency use authorization of the
drug for treating mild to moderate COVID-19 patients.
The U.S. government has committed that patients will have no
out-of-pocket costs for the medicine, although healthcare facilities
may charge a fee for the product's administration, Lilly said.
(Reporting by Manas Mishra in Bengaluru; Editing by Saumyadeb
Chakrabarty)
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