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To clarify, the timeframes during which the agency does not intend to take action against compounders for violations of the FD&C Act arising from conditions that depend on tirzepatide injection products inclusion on FDAs drug shortage list are: For a state-licensed pharmacy or physician compounding under section 503A of the FD&C Act until February 18, 2025, or until the date of the district courts decision on the plaintiffs preliminary injunction motion in Outsourcing Facilities Association (OFA) v

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The oral administration of NAC can substantially prevent the accumulation of -synuclein in cultured SH-SY5Y cells [78]

*Trial figures are group averages from studies of the FDA-approved branded medications, not compounded preparations