(Reuters) – Eli Lilly and Co
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)