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  • MFDS collects acetaminophen to confirm impurity
  • by Chon, Seung-Hyun | translator Byun Kyung A | Jul 28, 2020 06:33am
NRC reported risk of impurity in API manufactured by a Chinese-based company
Unacceptable level of impurity would inevitably and heavily impact the pharmaceutical industry
MFDS ¡°Investigating API as a preemptive action¡±
 ¡ã ½ÄǰÀǾàǰ¾ÈÀüó Àü°æ

The South Korean government is initiating an investigation on impurity contamination in an active pharmaceutical ingredient (API), acetaminophen. As the risk of impurity contamination in API manufactured by a Chinese manufacturer was raised recently, the government started proactively collecting and testing the API used in Korea. If the widely used acetaminophen were to be found with unacceptable level of impurity, the pharmaceutical industry would be unable to avoid a heavy blow.

According to pharmaceutical industry sources on July 27, Ministry of Food and Drug Safety (MFDS) has recently visited pharmaceutical companies and taken samples of acetaminophen to confirm the impurity contamination in the API.

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