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Reactions Weekly

, Volume 1761, Issue 1, pp 3–3 | Cite as

Losartan-containing tablets recalled due to NMBA impurity

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Reference

  1. US Food and Drug Administration. Macleods Pharmaceutical Limited Issues Voluntary Nationwide Consumer Level Recall of Losartan Potassium 50mg and Losartan Potassium/Hydrochlorothiazide combination Tablets 50mg/12.5mg, 100mg/12.5mg and 100mg/25mg due to detection of NMBA (N-Nitroso-N Methyl-4-aminobutyric acid) Impurity. Internet Document : 26 Jun 2019. Available from: URL: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/macleods-pharmaceutical-limited-issues-voluntary-nationwide-consumer-level-recall-losartan-potassium

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© Springer International Publishing AG 2019

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