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GJL Artesunate

NAFDAC Reg. No. C4-2017 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
GJL Artesunate
NAFDAC number
C4-2017
Active ingredient
Artesunate
Strength
60 mg
Form
Powder for injection
Pack size
1 x 1's (in vial) + Solvents (in ampoules)
Manufacturer
Not listed
Applicant (holder)
Grace Johnsons Limited
Approved
29 Sep 2022
Status
Active View on NAFDAC ↗
Registration valid to
28 Sep 2027
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • GJL Artesunate is on the NAFDAC register with an active registration (C4-2017). 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 GJL Artesunate

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

3 free checks left today Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About GJL Artesunate

What is in GJL Artesunate?

GJL Artesunate contains Artesunate (60 mg), as powder for injection, according to its NAFDAC registration record.

Is GJL Artesunate registered with NAFDAC?

Yes. GJL Artesunate is listed on the NAFDAC register under registration number C4-2017, and its registration is active as of 28 October 2026.

Has GJL Artesunate been flagged as fake or recalled?

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

How can I check that my pack of GJL Artesunate is genuine?

Run a free authenticity scan with the NAFDAC number C4-2017, 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.