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Made in Korea, it is given by intravenous or intramuscular administration and is often added alongside antioxidant IV protocols

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The firm acknowledged that releasing OOS compounded preparations reflects a deviation from internal quality assurance procedures and obligation to notify patients and prescribers. But the FDA found that no corrective actions were provided to address the failure to notify patients and prescribers when OOS results were identified

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It is prohibited by the WADA for its potential to enhance athletic performance

Food & Drug Administration, 2019, 2023, 2024)