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الرئيسية / Registered in Nigeria / Actrapid FlexPen 100 IU

Actrapid FlexPen 100 IU

NAFDAC Reg. No. A6-0449 · Drug

Registered with NAFDAC. Registration activeAs of 6 November 2026 · synced automatically from official sources.
Product
Actrapid FlexPen 100 IU
رقم NAFDAC
A6-0449
المادة الفعالة
Insulin regular (Human)
التركيز
300 units/3 mL
الشكل
Solution for injection
حجم العبوة
3 mL x 5's (in pre-filled multidose disposable pen)
Manufacturer
Not listed
Applicant (holder)
Novo Nordisk Pharma Ltd
Approved
3 Oct 2022
الحالة
Active View on NAFDAC ↗
التسجيل ساري حتى
2 Oct 2027
تنبيهات منظمة الصحة العالمية
None found
Community reports
None
Times checked
0

About the medicine: Insulin regular: uses, dosage and brands worldwide

What we found

  • Actrapid FlexPen 100 IU is on the NAFDAC register with an active registration (A6-0449). 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 Actrapid FlexPen 100 IU

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

لمن هو

INDICATIONS For the temporary relief of general weakness, debilitation, excessive sweating, or minor skin rash or hives due to sensitivity to phenolic compounds found in foods or other products.*

كيف يُتناول وكم مرة
  • Place drops under tongue 30 minutes before/after meals
  • Adults and children 12 years and over: Take 10 drops up to 3 times per day
  • Consult a physician for use in children under 12 years of age
Warnings

In case of overdose, get medical help or contact a poison control center right away. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.

Pregnancy and breastfeeding

If pregnant or breastfeeding, ask a healthcare professional before use.

How to store it

Keep out of reach of children.

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 2026-01-08.

Label for insulin regular (human), the active ingredient registered with NAFDAC.

Check your pack of Actrapid FlexPen 100 IU

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

أو التقط صورًا للعبوة
تبقّت 3 عمليات تحقق مجانية اليوم Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Actrapid FlexPen 100 IU

What is in Actrapid FlexPen 100 IU?

Actrapid FlexPen 100 IU contains Insulin regular (Human) (300 units/3 mL), as solution for injection, according to its NAFDAC registration record.

Is Actrapid FlexPen 100 IU registered with NAFDAC?

Yes. Actrapid FlexPen 100 IU is listed on the NAFDAC register under registration number A6-0449, and its registration is active as of 6 November 2026.

Has Actrapid FlexPen 100 IU been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Actrapid FlexPen 100 IU in our automatically synced alert list.

How can I check that my pack of Actrapid FlexPen 100 IU is genuine?

Run a free authenticity scan with the NAFDAC number A6-0449, 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 Actrapid FlexPen 100 IU?

Follow your prescription or the leaflet in your pack. The official label says: Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.…

What is Actrapid FlexPen 100 IU used for?

INDICATIONS For the temporary relief of general weakness, debilitation, excessive sweating, or minor skin rash or hives due to sensitivity to phenolic compounds found in foods or other products.* (Summarised from the official U.S. FDA label for insulin regular (human). 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.