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Actrapid 100 IU/mL Vial

NAFDAC Reg. No. A6-0069 · Drug

Registered with NAFDAC — registration activeAs of 6 November 2026 · synced automatically from official sources.
Product
Actrapid 100 IU/mL Vial
NAFDAC number
A6-0069
Active ingredient
Insulin regular (Human)
Strength
1000 units/10 mL
Form
Solution for injection
Pack size
10 mL x 1’s (in glass vial)
Manufacturer
Not listed
Applicant (holder)
Novo Nordisk Pharma Ltd
Approved
28 Aug 2021
Status
Inactive View on NAFDAC ↗
Registration valid to
27 Aug 2026
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Actrapid 100 IU/mL Vial is on the NAFDAC register with an active registration (A6-0069). 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. Not medical advice — always follow your doctor or pharmacist.

What Actrapid 100 IU/mL Vial is used for

From the official U.S. FDA label for insulin regular (human), the active ingredient registered with NAFDAC.

What it is 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.*

Purpose

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

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 & breastfeeding

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

General information only — not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

Check your pack of Actrapid 100 IU/mL Vial

Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.

3 free checks left today · no signup Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Actrapid 100 IU/mL Vial

What is in Actrapid 100 IU/mL Vial?

Actrapid 100 IU/mL Vial contains Insulin regular (Human) (1000 units/10 mL), as solution for injection, according to its NAFDAC registration record.

Is Actrapid 100 IU/mL Vial registered with NAFDAC?

Yes. Actrapid 100 IU/mL Vial is listed on the NAFDAC register under registration number A6-0069, and its registration is active as of 6 November 2026.

Has Actrapid 100 IU/mL Vial been flagged as fake or recalled?

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

How can I check that my pack of Actrapid 100 IU/mL Vial is genuine?

Run a free authenticity scan with the NAFDAC number A6-0069, 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.

What is Actrapid 100 IU/mL Vial 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 RxVerify users, not medical advice. Report side effects to your doctor and to NAFDAC.