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FDA received another adverse event report on February 4, 2019, associated with an intravenous injection of a drug containing L-glutathione 200mg/mL compounded by a different pharmacy that also used L-glutathione repackaged by Letco (lot number: 1808030045, expiration date: 6/17/2020)
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10.1002/1521-3765(20010803)7:15 3.0.CO;2-7 Chemistry 105 KiziltepeT.HideshimaT.IshitsukaK.OcioE
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