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Afriject

NAFDAC REG NO: 03-8040 Médicament

Enregistré auprès de NAFDAC. Enregistrement actifAs of 29 October 2026 · synced automatically from official sources.
Produit
Afriject
Numéro NAFDAC
03-8040
Principe actif
Syringes and Needles
Dosage
N/A
Forme
N/A
Conditionnement
2 mL x 100's
Fabricant
Non répertorié
Déposant / Titulaire :
Mikano International Limited
Approuvé
29 Mar 2023
Statut
Actif Vue sur NAFDAC ↗
Enregistrement valable jusqu'au
28 Mar 2028
Alertes OMS
Non trouvé
Community reports
None
Times checked
0

About the medicine: Syringes: uses, dosage and brands worldwide

What we found

  • Afriject is on the NAFDAC register with an active registration (03-8040). 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 Afriject

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

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Encore 3 vérifications gratuites aujourd'hui Sources officielles : FDA américaine · EMA (UE) · NAFDAC · alertes OMS

About Afriject

What is in Afriject?

Afriject contains Syringes and Needles (NA), as na, according to its NAFDAC registration record.

Is Afriject registered with NAFDAC?

Yes. Afriject is listed on the NAFDAC register under registration number 03-8040, and its registration is active as of 29 October 2026.

Has Afriject been flagged as fake or recalled?

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

How can I check that my pack of Afriject is genuine?

Run a free authenticity scan with the NAFDAC number 03-8040, 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.