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Securing FDA approval requires the submission of pre-clinical, clinical and/or pharmacokinetic data, information about product manufacturing processes and inspection of facilities and supporting information to the FDA for each therapeutic indication to establish a product candidates safety and efficacy for each indication

The Company has determined the probability from December 31, 2022 to December 31, 2023 has decreased from A roll forward of the fair value of the derivative liability for the year ended December 31, 2023 is presented below

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Complementary Inactive Ingredients While semaglutide is the star, PharmaZee's compounded formulations may also include stabilizing agents, buffers, or delivery-optimized carriers (depending on oral or injectable form)