Bilaxten 20 mg Tablet — NAFDAC C4-0657: Is It Genuine? Uses, Alerts

Ọja: Bilaxten 20 mg Tablet
Nọmba NAFDAC: C4-0657
Ohun elo ti nṣiṣe lọwọ: Bilastine
Agbara: 20 mg
Fọọmu: Tablet
Iwọn iṣakojọpọ: 1 x 10's (in Alu-PVC blister)
Olupese: Ko ṣe atokọ
Olubẹwẹ (oluranlowo): Faes Farma Nigeria Limited
Ti fọwọsi: 27 May 2025
Ipò: Nṣiṣẹ Wo lórí NAFDAC ↗
Iforukọsilẹ wulo si: 26 May 2030
Tani o ṣe itaniji: Kosi ikankan ti a rii.
Ijabọ Agbegbe: Kò sí
Àwọn àyẹ̀wò àsìkò: 0

Nipa oogun naa: Bilastine: uses, dosage and brands worldwide

What we found

Bilaxten 20 mg Tablet is on the NAFDAC register with an active registration (C4-0657). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

Check your pack of Bilaxten 20 mg Tablet

Add the expiry date on your pack for a full Trust Score.

3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

About Bilaxten 20 mg Tablet

What is in Bilaxten 20 mg Tablet?

Bilaxten 20 mg Tablet contains Bilastine (20 mg), as tablet, according to its NAFDAC registration record.

Is Bilaxten 20 mg Tablet registered with NAFDAC?

Yes. Bilaxten 20 mg Tablet is listed on the NAFDAC register under registration number C4-0657, and its registration is active as of 1 November 2026.

Has Bilaxten 20 mg Tablet been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Bilaxten 20 mg Tablet in our automatically synced alert list.

How can I check that my pack of Bilaxten 20 mg Tablet is genuine?

Run a free authenticity scan with the NAFDAC number C4-0657, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

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Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.