NAFDAC Drug And Drug Product Labelling Regulations 2019
Ministry of Industry, Trade and Investment, Nigeria
These regulations shall apply to all labelling of drugs. Except as provided in these regulations, no person shall manufacture, import, export, distribute, advertise, display for sale or use any drug or drug product unless it is labelled per these regulations. It outlines labelling information, declaration of content of ingredients under composition, labelling of over-the-counter drugs and registration number assigned by the agency.
Process Flow
Department of Drug Evaluation and Research ⬤
Office of the Director General NAFDAC ⬤
Office of the Permanent Secretary, Ministry of Health ⬤
Office of the Minister of State for Health ⬤
Office of the Minister of Health ⬤
Federal Executive Council ⬤
NAFDAC Drug And Drug Product Labelling Regulations 2019 Current Version
January 2022
These regulations shall apply to all labelling of drugs. Except as provided in these regulations, no person shall manufacture, import, export, distribute, advertise, display for sale or use any drug or drug product unless it is labelled per these regulations. It outlines labelling information, declaration of content of ingredients under composition, labelling of over-the-counter drugs and registration number assigned by the agency.
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