Drug and Related Product Labelling Regulations 2019
Ministry of Health, National Agency for Food and Drug Administration and Control, Nigeria
These regulations apply to all labelling of drugs and related products manufactured, imported, exported, sold, distributed or used in Nigeria. No person can manufacture, import, export, distribute, advertise, display for sale or use any drug or drug product unless it is labelled in accordance with these regulations.
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 for Health ⬤
Contacts
Ijeoma U. Nwankwo
Director
National Agency for Food and Drug Administration and Control (NAFDAC)
Moji Adeyeye
Director General
National Agency for Food and Drug Administration and Control (NAFDAC)
Mahmuda Mamman
Permanent Secretary
Ministry of Health
Adeleke O. Mamora
Honourable Minister of State
Ministry of Health
Osagie Ehanire
Honourable Minister
Ministry of Health
Drug and Related Product Labelling Regulations 2019 Current Version
January 2022
These regulations apply to all labelling of drugs and related products manufactured, imported, exported, sold, distributed or used in Nigeria. No person can manufacture, import, export, distribute, advertise, display for sale or use any drug or drug product unless it is labelled in accordance with these regulations.
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