Merck Provides U.S. Regulatory Update on Sugammadex Sodium Injection
March 14, 2013 5:16 pm ET
WHITEHOUSE STATION, N.J., March 14, 2013 – Merck (NYSE:MRK), known as MSD outside the United States and Canada, today announced that the U.S. Food and Drug Administration (FDA) has notified Merck that the agency will take an additional three months to review the New Drug Application (NDA) resubmission for sugammadex sodium injection. Merck anticipates the FDA’s review will be completed in the second half of 2013.
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