Regulatory Directives

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Regulatory Directives

Regulatory directives (RDs) are official instructions or guidelines issued by NAFDAC. The key purpose is to provide clarity and detailed instructions on a particular regulatory framework to facilitate stakeholder’s compliance. This will promote best practices, compliance with laws and regulations and maintain standards across different industries and sectors. RDs rely on Regulatory Intelligence to promote continual improvement and adaptation to new/emerging safety issues, technologies, and regulatory practices.

Regulatory directives play a vital role in, protecting stakeholders, and promoting a rational, cordial, and efficient regulatory environment that will safeguard the health of the public.

Date	Title
04-Jul-24	Regulatory Directive on Discontinued Registration of Aceclofenac Sodium 100mg, Paracetamol 500mg, Chlorzaxone 250mg Fixed Dose Combination
04-Jul-24	Regulatory Directive on Discontinued Registration of Diclofenac Sodium 50mg, Paracetamol 325mg, Chlorzoxazone 250mg Fixed Dose Combination
04-Jul-24	Regulatory Directive on the Registration of Cyproheptadine 2mg & 4mg in combination with Multivitamin formulations
08-Jul-24	Regulatory Directive on Discontinued Registration of Aceclofenac Sodium 100mg, Paracetamol 500mg, Chlorzaxone 250mg Fixed Dose Combination
08-Jul-24	Regulatory Directive on Discontinued Registration of Analgin or Novalgin (Generic Metamizole) Formulations
08-Jul-24	Regulatory Directive on Discontinued Registration of Chloroquine Injection
08-Jul-24	Regulatory Directive on Discontinued Registration of Diclofenac Potassium 100mg
08-Jul-24	Regulatory Directive on Discontinued Registration of Diclofenac Sodium 50mg, Paracetamol 325mg, Chlorzoxazone 250mg Fixed Dose Combination
08-Jul-24	Regulatory Directive on Discontinued Registration of Halofantrine Tablet (1)
08-Jul-24	Regulatory Directive on Discontinued Registration of Ketoconazole tablet
08-Jul-24	Regulatory Directive on Discontinued Registration of Multi-dose Antimalaria Oral Suspensions
08-Jul-24	Regulatory Directive on NAFDAC Regulated Products on ceiling List
08-Jul-24	Regulatory Directive on the Registration of Cyproheptadine 2mg & 4mg in combination with Multivitamin formulations

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Content Current as of July 8, 2024

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NATIONAL AGENCY FOR FOOD AND DRUG ADMINISTRATION AND CONTROL (NAFDAC)

This is the Official Website of Nafdac, the Agency commissioned to protect and promote the public health by instituting an effective and efficient regulatory system that ensures only the right quality food, drugs and other regulated products are manufactured, exported, imported, advertised, distributed, sold, and used