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The series of the drug "Telsartan N" manufactured in India is being recalled.

In some series sold in Uzbekistan, the amount of active substance exceeding the norm has been identified.

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According to the Center for the Safety of Pharmaceutical Products, the amount of hydrochlorothiazide in the C2501976 series of the drug "Telsartan H 80 mg/12.5 mg" manufactured by India's "Dr. Reddy's Laboratories Ltd" has deviated from the established norm. Consequently, this series of the drug is being recalled from circulation. 

No non-conformity has been identified in the C2501977 series, but as a precautionary measure, it is also being withdrawn from the market. Citizens are advised not to use this drug and, if necessary, to choose an alternative medication after consulting a doctor.

The Center urges the public to handle medications based on information verified from official sources.

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