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This is to ensure that compounders do not evade the limits in this section by making relatively small changes to a compounded drug product and then offering the drug to the general public without regard to whether a prescribing practitioner has determined that the change produces for the patient a significant difference. In other words, under this broad interpretation, the statute would appear to deem subcutaneous semaglutide injectable drugs essentially copies irrespective whether one product was formulated with semaglutide base and the other with semaglutide salt

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