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Amosinin Tablets

NAFDAC Reg. No. C4-1156 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Amosinin Tablets
NAFDAC number
C4-1156
Active ingredient
Dihydroartemisinin; Piperaquine Phosphate
Strength
40 mg; 320 mg
Form
Tablet
Manufacturer
Not listed
Applicant (holder)
Astra Pharma Ltd
Approved
10 Nov 2020
Status
Inactive View on NAFDAC ↗
Registration valid to
9 Nov 2025
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Amosinin Tablets is on the NAFDAC register with an active registration (C4-1156). 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 Amosinin Tablets

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 Amosinin Tablets

What is in Amosinin Tablets?

Amosinin Tablets contains Dihydroartemisinin; Piperaquine Phosphate (40 mg; 320 mg), as tablet, according to its NAFDAC registration record.

Is Amosinin Tablets registered with NAFDAC?

Yes. Amosinin Tablets is listed on the NAFDAC register under registration number C4-1156, and its registration is active as of 28 October 2026.

Has Amosinin Tablets been flagged as fake or recalled?

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

How can I check that my pack of Amosinin Tablets is genuine?

Run a free authenticity scan with the NAFDAC number C4-1156, 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.