Merck Seeks FDA Authorization for Antiviral COVID-19 Pill

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Merck Seeks FDA Authorization for Antiviral COVID-19 Pill
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Drugmaker Merck has submitted an application to the FDA for emergency use authorization of its antiviral COVID-19 pill.

manufacturers in India to provide molnupiravir to more than 100 low- and middle-income countries after approval from local regulatory agencies.

Merck: “Merck and Ridgeback Announce Submission of Emergency Use Authorization Application to the U.S.

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