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India to force drugmakers to upgrade plants after fatal cough syrup crisis

India mandates all drugmakers meet WHO manufacturing standards after toxic cough syrup with 49% diethylene glycol caused 24 child deaths, sparking arrests and bans.

  • On Oct 16, India refused drugmakers' requests to extend a year-end deadline to upgrade facilities to WHO standards after tests confirmed toxic Coldrif batches.
  • Government laboratory results showed 48.6 per cent diethylene glycol in the Sresan Pharmaceutical Manufacturer's May Coldrif batch, which IPC materials say can be 'fraudulently or unintentionally' used.
  • Regional drug inspectors collected samples while at least four pharmacies closed temporarily, community health workers retrieved Coldrif bottles door-to-door, and local physician Praveen Soni was arrested in the probe.
  • Amid public outrage, at least 24 children have died after taking the syrup, intensifying anger and damaging India's international reputation as a 'pharmacy of the world' after linked deaths in Africa and Central Asia.
  • India's US$50 billion pharmaceutical industry, with about 3,000 companies operating over 10,000 factories, faces warnings that nearly 49% of Himachal Pradesh units could close without extensions, risking shortages.
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groundreport.in broke the news in on Thursday, October 16, 2025.
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