The National Agency for Food and Drug Administration and Control (NAFDAC) has notified Nigerians of the sale of counterfeit Combiart (Artemether Lumefantrine 20/120mg) Dispersible Tablet in Nigeria.
The notification issued on NAFDAC’s website disclosed the date of manufacturing of the drug to be February 2023 and June 2023.
It equally gave the expiring date of the drug as May 2026 and June 2026, as well as batch no: 7225119 with NAFDAC Reg No: A11-0299.
NAFDAC gave the manufacturer name and address as Strides Arcolab Limited, 36/7, Suragajakkanahalli, Indlavadi Cross, Anekal Taluk, Bangalore- 562 106, India.
NAFDAC, in the alert, said all its zonal directors and state coordinators had been directed to carry out surveillance and mop up the counterfeit products within the zones and states.
It advised importers, distributors, retailers, healthcare professionals, and caregivers to exercise caution and vigilance within the supply chain and avoid importation, distribution, sale, and usage of counterfeit product.
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The agency said all medical products must be obtained from authorised/licenced suppliers and that products’ authenticity and physical condition must be carefully checked.
NAFDAC also urged healthcare professionals and consumers to report any suspicion of the sale of substandard and falsified medicines or medical devices to the nearest agency’s office.
It urged Nigerians to call NAFDAC on 0800-162-3322 or report any suspicion event via email: sf.alert@nafdac.gov.ng.
“Healthcare professionals and patients are similarly encouraged to report adverse or side effects related to the use of medicinal products or devices to the nearest NAFDAC office, or through E-reporting platforms available on the NAFDAC website www.nafdac.gov.ng,” the agency said.
NAFDAC added that the notice would be uploaded to the WHO Global Surveillance and Monitoring System (GSMS).
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