Last Updated:2025/11/24

An ANDA was submitted last month to the FDA to request approval for a generic version of the drug.

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An ANDA was submitted last month to the FDA to request approval for a generic version of the drug.

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先月、略式新薬申請がジェネリック薬の承認を求めるために米国食品医薬品局(FDA)に提出されました。

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