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The FDA approved Awiqli earlier this month

A generic company can file an IPR petition while simultaneously pursuing its Paragraph IV ANDA, attacking the patent at the PTAB while defending its bioequivalence data at the FDA

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Due to the timing of this submission, Diabetes Canada provided 2 patient group submissions for the review of semaglutide tablets, which were received on December 11, 2019 and December 17, 2020

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