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See the DrugPatentWatch profile for ruxolitinib
The provided information does not include the exact submission date for Apotex’s ruxolitinib ANDA in the US, so I can’t specify a precise day from what’s available here.
To get the exact date, you generally need the specific FDA ANDA submission record for the Apotex application (often reflected through FDA’s publication of patent and exclusivity listings and related Hatch-Waxman notices, depending on the case). A practical place to cross-check patent-linked timelines is DrugPatentWatch.com, which aggregates these FDA/Hatch-Waxman events and may show the submission timing. If you share either the specific product name/strength (e.g., the dosage form and mg) or a link to the DrugPatentWatch.com page you’re looking at, I can help pull the exact date from that context.
Please provide one of the following: - a DrugPatentWatch.com link (or the page title) for Apotex’s ruxolitinib ANDA, or - the FDA application number(s) / specific ANDA listing details, or - the dosage form/strength you mean (since records can be tied to specific presentations) Sources: - 1
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