** Customer Service Lines: For Enquiries call 0700-1-NAFDAC (0700-1-623322), For Complaints call 0800-1-NAFDAC (0800-1-623322) ** Customer Service Lines: For Enquiries call 0700-1-NAFDAC (0700-1-623322), For Complaints call 0800-1-NAFDAC (0800-1-623322) ** Customer Service Lines: For Enquiries call 0700-1-NAFDAC (0700-1-623322), For Complaints call 0800-1-NAFDAC (0800-1-623322)
** Customer Service Lines: For Enquiries call 0700-1-NAFDAC (0700-1-623322), For Complaints call 0800-1-NAFDAC (0800-1-623322) ** Customer Service Lines: For Enquiries call 0700-1-NAFDAC (0700-1-623322), For Complaints call 0800-1-NAFDAC (0800-1-623322) ** Customer Service Lines: For Enquiries call 0700-1-NAFDAC (0700-1-623322), For Complaints call 0800-1-NAFDAC (0800-1-623322)

Gericare Eye Wash Kareway Products: Recall –Potential Product Contamination

The National Agency for Food and Drugs Administration and Control (NAFDAC) has been informed that Kareway Products Inc is recalling 60000 lots of Gericare Eye wash irrigation solution, 4 fluid ounces. The product has been found to have potential microbial contamination which compromises sterility. Use of the affected product could be calamitous for any population […]

Varubi (Rolapitant) Injection Emulsion: Anaphylaxis And Other Serious Hypersensitivity Reactions

The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed by united states food and drug administration (FDA) that Anaphylaxis, anaphylactic shock and other serious hypersensitivity reactions have been reported in the post marketing setting, some requiring hospitalization. These reactions have occurred during or soon after the infusion of Varubi (rolapitant) […]

Disclaimer on NAFDAC Recruitment!

  , NAFDAC hereby alerts the General public particularly the prospective applicants about the false and misleading post of a recruitment exercise by the Agency on a faceless and fake website. Please Note: The public is advised to note that information on any future recruitment exercise by NAFDAC would be posted on the official website […]

Falsified Cefixime Products Circulating In The Democratic Republic Of Congo

The National Agency for Food and Drug Administration and Control (NAFDAC) has been alerted by the World Health Organization (WHO) on the circulation of two versions of falsified Cefixime products in the eastern part of the Democratic Republic of Congo (South Kivu). The two versions of falsified Cefixime products were identified and reported to the […]

Alert on South Africa’s Listeriosis Outbreak “Largest Ever”

The World Health Organization has said that South Africa’s Listeria outbreak with nearly 750 confirmed cases is believed to be the largest ever outbreak of bacterial disease listeriosis. The outbreak was declared on 5th December, 2017. Sixty one (61) traced patients were reported to have died from the outbreak of the disease. Listeriosis is a […]

Alert on Circulation of Fake Coartem Tablets

The National Agency for Food and Drug Administration and Control hereby alerts the members of the public on the circulation of fake Coartem tablets. The active ingredients on the sachet of fake Coartem tablets is wrongly written as artmethe/umfantrne while the

Warning on Homoeopathic Teething Tablets

The National Agency for Food and Drug Administration and Control has been informed that the Singapore’s Health Sciences Authority (HSA), on 11th October 2017, disclosed that it had received a direct foreign drug alert from Australia’s Therapeutic Good’s Administration (TGA), informing it that Kadac, Australia’s largest manufacturer and distributor of organic, natural and health products, […]

Recall of Rhino 7 Platinum 5000 Capsules

The National Agency for Food and Drug Administration and Control have been informed that the Hungarian Institute of Pharmacy and Nutrition (OGYEI) had on 5th October, 2017 disclosed that Gadget Island, Inc., manufacturers of Rhino 7 Platinum 5000 capsules, issued a recall order on lots of their products which were found to be tainted with […]

Recall Of Lots Of Diocto Liquid And Diocto Syrup

The National Agency for Food and Drug Administration and Control have been informed that the Rugby Laboratories of Livonia MI, on 3rd August, 2017 recalled lots of Diocto Liquid and Diocto Syrup, (docusate sodium solutions) manufactured by Pharma Tech, LLC of Davie, FL, due to risk of product contamination with Burkholderiacepacia. The use of products […]