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Fanexin Tablet

NAFDAC Reg. No. A4-9126 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Fanexin Tablet
NAFDAC number
A4-9126
Active ingredient
Dihydroartemisinin; Piperaquine Phosphate
Strength
40 mg; 320 mg
Form
Tablet
Manufacturer
Not listed
Applicant (holder)
Hanbet Pharmaceuticals Limited
Approved
21 Dec 2020
Status
Inactive View on NAFDAC ↗
Registration valid to
20 Dec 2025
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Fanexin Tablet is on the NAFDAC register with an active registration (A4-9126). 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 Fanexin Tablet

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

3 free checks left today Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Fanexin Tablet

What is in Fanexin Tablet?

Fanexin Tablet contains Dihydroartemisinin; Piperaquine Phosphate (40 mg; 320 mg), as tablet, according to its NAFDAC registration record.

Is Fanexin Tablet registered with NAFDAC?

Yes. Fanexin Tablet is listed on the NAFDAC register under registration number A4-9126, and its registration is active as of 28 October 2026.

Has Fanexin Tablet been flagged as fake or recalled?

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

How can I check that my pack of Fanexin Tablet is genuine?

Run a free authenticity scan with the NAFDAC number A4-9126, 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.