NAFDAC Withdraws Approvals for 101 Products in Nigeria

The National Agency for Food and Drug Administration Control (NAFDAC) has announced the withdrawal, suspension, and cancellation of approvals for multiple products in Nigeria. In a statement on its official website, NAFDAC listed 101 products whose registrations have been affected, including various tablets, eye drops, injections, and suspensions.

The agency stated that these products are no longer authorized for manufacturing, importation, exportation, distribution, or sale in the country. NAFDAC clarified that the withdrawal or suspension of product registrations may occur if the market authorization holder discontinues use voluntarily or fails to meet required conditions.

The action is part of NAFDAC's regulatory efforts to ensure the safety and efficacy of products available in the Nigerian market.