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Table 6 summarizes all the nanoparticles used for neuroprotection in PD treatment

Specifically, the panel will assess whether those substances should be moved off the Category 2 list a designation reserved for bulk drug substances that present potential safety risks and are therefore ineligible for routine compounding under Section 503A of the Federal Food, Drug, and Cosmetic Act

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The black dots represent individual prevalence rates, which were aggregated to yield an overall pooled prevalence of 41%