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  5. Public Alert No. 023/2025 – Recall of Multivitamin Supplements due to Risk of Serious Injury…

Public Alert No. 033/2025 – Alert on the Sale of Counterfeit Cialis Tablet 20mg in Nigeria

The National Agency for Food and Drug Administration and Control (NAFDAC) is alerting the public about the distribution and sale of counterfeit Cialis 20mg tablets in Nigeria.

Information received from the Marketing Authorization Holder (MAH) shows that the counterfeit version was discovered during a routine market surveillance in Abuja.

It was reported that the counterfeit Cialis 20mg tablets are being sold openly in the market at an average price of ₦8,000 per pack, contrary to the genuine product, which is retailed at about ₦55,000 per pack. Further examination of the counterfeit product showed that it is not consistent with the authentic Cialis 20mg packaging and quality specifications.

Genuine Cialis 20mg Tablet contains tadalafil, which is used to treat erectile dysfunction (ED) in men and pulmonary arterial hypertension (PAH). 

Product details             

The details of the counterfeit Cialis 20mg tablets versus the genuine ones are as follows.

Product Details

Genuine

Counterfeit

Product Name

Cialis 20mg film-coated tablets

Cialis Tadalafil tablets 20mg

Stated NRN

04-5196

4464

Manufacturing Date

03 2023

03/2024

Expiring Date

02 2026

02/2027

Lot. No

D636431

E3242401

Product photo

All NAFDAC zonal directors and state coordinators have been directed to carry out surveillance and mop up the counterfeit product within the zones and states.

Importers, distributors, retailers, healthcare professionals, and caregivers are advised to exercise caution and vigilance in the supply chain to prevent the importation, distribution, sale, and use of counterfeit products. All medical products must be obtained from authorized/licensed suppliers. The products’ authenticity and physical condition should be carefully checked.

Healthcare professionals and consumers are advised to report any suspicion of the sale of substandard and falsified medicines or medical devices to the nearest NAFDAC office, NAFDAC on 0800-162-3322, or via email: sf.alert@nafdac.gov.ng

Similarly, healthcare professionals and patients are also encouraged to report adverse events or side effects related to the use of medicinal products or devices to the nearest NAFDAC office, or through the use of the E-reporting platforms available on the NAFDAC website www.nafdac.gov.ng, or via the Med-safety application available for download on Android and IOS stores, or via e-mail on pharmacovigilance@nafdac.gov.ng

Furthermore, note that this notice will be uploaded to the WHO Global Surveillance and Monitoring System (GSMS).

NAFDAC………. Customer-focused, Agency-minded!!!

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