The Nationwide Company for Meals and Drug Administration and Management (NAFDAC) has introduced the instant withdrawal, suspension, and cancellation of 101 pharmaceutical merchandise.
The meals and drug regulator stated that these pharmaceutical merchandise are now not permitted for manufacture, importation, exportation, distribution, commercial, sale and use inside Nigeria.
This disclosure is contained in an announcement issued by NAFDAC on its X (previously Twitter) official deal with on Tuesday, September 30, 2025, the place it said that the checklist of those merchandise might be accessed on its web site.
The checklist covers a whole bunch of things throughout medicines and well being merchandise from antimalarials (varied artemether/lumefantrine formulations) and cardiovascular medicine (valsartan merchandise) to insulin/growth-hormone injectables (Norditropin), diabetes medicines (Januvia/Janumet), inhalers and eye drops.
The checklist contains some broadly used medicine like Abacavir tablets, Amaryl tablets, Aprovasc tablets, Artemether/Lumefantrine, ASAQ(Artesunate amodiaquine Winthrop) 100mg/270mg Tablets, ASAQ(Artesunate amodiaquine Winthrop) 25mg/67.5mg Tablets, Mixture 3 Tablets, Amlodipine, amongst many others.
The merchandise are from some well-known pharmaceutical firms like Sanofi Aventis Nigeria ltd, Novartis Nigeria Restricted, Bayer East Africa Restricted, Healthline Restricted, Fensyl MHP Consulting Ltd, and lots of others.
The whole checklist of the 101 merchandise and the pharmaceutical firms might be seen .
What NAFDAC is saying
NAFDAC, in its assertion, stated, ‘’That is to tell the Basic Public that the next merchandise are accredited for withdrawal, suspension and cancellation by NAFDAC. They’re due to this fact now not permitted for manufacture, importation, exportation, distribution, commercial, sale and use inside Nigeria.
‘’Please word that: The Certificates of Registration of a product is alleged to be withdrawn when using the Certificates of Registration of that product is discontinued upon request of the Market Authorisation Holder.
The Certificates of Registration of a product could also be suspended when the circumstances upon which the NAFDAC Registration license was issued are now not met, and the Company is to make a dedication.
The Certificates of Registration of a product is alleged to be cancelled when the NAFDAC Certificates of Registration license of that product is revoked by NAFDAC.’’
What you need to know
The motion by NAFDAC amid rising international issues over pretend and substandard medicines which has develop into a menace.
Substandard and falsified medical merchandise are a big international well being downside, impacting tens of millions of individuals and compromising well being techniques worldwide. These merchandise might be present in all international locations, impacting all forms of medical merchandise, together with life-saving remedies like vaccines, antibiotics and most cancers therapies.
The World Well being Group (WHO) had, in a report a number of years in the past, estimated that 1 in 10 medicines in low- and middle-income international locations failed high quality management exams, suggesting the product is substandard or falsified.
In a associated growth, NAFDAC had a couple of days in the past sought the collaboration of pharmacists to sort out the problem of substandard and falsified medicines.
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