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الرئيسية / Registered in Nigeria / Panbio COVID-19 Ag Rapid Test Device (Nasal)

Panbio COVID-19 Ag Rapid Test Device (Nasal)

NAFDAC Reg. No. A3-100907 · Drug

Registered with NAFDAC. Registration activeAs of 2 November 2026 · synced automatically from official sources.
Product
Panbio COVID-19 Ag Rapid Test Device (Nasal)
رقم NAFDAC
A3-100907
المادة الفعالة
COVID-19 Test
التركيز
NA
الشكل
NA
حجم العبوة
1 x 25's (Tests in a box)
Manufacturer
Not listed
Applicant (holder)
Abbott Healthcare Nigeria Limited
Approved
24 Feb 2023
الحالة
Active View on NAFDAC ↗
التسجيل ساري حتى
22 Feb 2028
تنبيهات منظمة الصحة العالمية
None found
Community reports
None
Times checked
0

About the medicine: Covid-: uses, dosage and brands worldwide

What we found

  • Panbio COVID-19 Ag Rapid Test Device (Nasal) is on the NAFDAC register with an active registration (A3-100907). 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.

How to use Panbio COVID-19 Ag Rapid Test Device (Nasal)

ما تقوله النشرة الرسمية. إذا وصفه لك طبيب، فاتبع الوصفة. وإذا اختلفت نشرة عبوتك، فالأولوية لها.

لمن هو

Dilute with 5g of oil in 500ml of water

كيف يُتناول وكم مرة

for topical use only

Warnings

Do not drink. Beware of fire. Keep out of reach of children. Avoid direct sunlight. Do not use directly on the skin

إذا نسيت جرعة

تناولها عندما تتذكر، إلا إذا اقترب موعد الجرعة التالية. عندها تخطَّ الجرعة المنسية. لا تتناول جرعتين معًا أبدًا للتعويض. راجع النشرة، فبعض الأدوية مختلفة.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2020-08-01.

Label for covid-, the active ingredient registered with NAFDAC.

Check your pack of Panbio COVID-19 Ag Rapid Test Device (Nasal)

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 Panbio COVID-19 Ag Rapid Test Device (Nasal)

What is in Panbio COVID-19 Ag Rapid Test Device (Nasal)?

Panbio COVID-19 Ag Rapid Test Device (Nasal) contains COVID-19 Test (NA), as na, according to its NAFDAC registration record.

Is Panbio COVID-19 Ag Rapid Test Device (Nasal) registered with NAFDAC?

Yes. Panbio COVID-19 Ag Rapid Test Device (Nasal) is listed on the NAFDAC register under registration number A3-100907, and its registration is active as of 2 November 2026.

Has Panbio COVID-19 Ag Rapid Test Device (Nasal) been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Panbio COVID-19 Ag Rapid Test Device (Nasal) in our automatically synced alert list.

How can I check that my pack of Panbio COVID-19 Ag Rapid Test Device (Nasal) is genuine?

Run a free authenticity scan with the NAFDAC number A3-100907, 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.

How do I take Panbio COVID-19 Ag Rapid Test Device (Nasal)?

Follow your prescription or the leaflet in your pack. The official label says: for topical use only…

What is Panbio COVID-19 Ag Rapid Test Device (Nasal) used for?

Dilute with 5g of oil in 500ml of water (Summarised from the official U.S. FDA label for covid-. Always follow your doctor or pharmacist.)

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