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Afriject

NAFDAC Reg. No. 03-8040 · Drug

Registered with NAFDAC. Registration activeAs of 1 November 2026 · synced automatically from official sources.
Product
Afriject
رقم NAFDAC
03-8040
المادة الفعالة
Syringes and Needles
التركيز
NA
الشكل
NA
حجم العبوة
2 mL x 100's
Manufacturer
Not listed
Applicant (holder)
Mikano International Limited
Approved
29 Mar 2023
الحالة
Active View on NAFDAC ↗
التسجيل ساري حتى
28 Mar 2028
تنبيهات منظمة الصحة العالمية
None found
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.

أو التقط صورًا للعبوة
تبقّت 3 عمليات تحقق مجانية اليوم المصادر الرسمية: FDA الأمريكية · EMA (الاتحاد الأوروبي) · NAFDAC · تنبيهات منظمة الصحة العالمية

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 1 November 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.