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SPAQ-Co Dispersible Tablets 500 mg/25 mg/153 mg

NAFDAC Reg. No. B4-6482 · Drug

Registered with NAFDAC — registration activeAs of 6 November 2026 · synced automatically from official sources.
Product
SPAQ-Co Dispersible Tablets 500 mg/25 mg/153 mg
NAFDAC number
B4-6482
Active ingredient
Amodiaquine (Amodiaquine Hydrochloride); Sulfadoxine; Pyrimethamine
Strength
153 mg; 500 mg; 25 mg
Form
Dispersible tablet
Pack size
50 x 4's (combipack of 1 Amodiaquine tablet + 3 Sulfadoxine/Pyrimethamine tablets in PVC/Alu blisters)
Manufacturer
Not listed
Applicant (holder)
Tridem Pharma Nigeria Limited
Approved
28 Mar 2023
Status
Active View on NAFDAC ↗
Registration valid to
27 Mar 2028
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • SPAQ-Co Dispersible Tablets 500 mg/25 mg/153 mg is on the NAFDAC register with an active registration (B4-6482). 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.

Check your pack of SPAQ-Co Dispersible Tablets 500 mg/25 mg/153 mg

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 SPAQ-Co Dispersible Tablets 500 mg/25 mg/153 mg

What is in SPAQ-Co Dispersible Tablets 500 mg/25 mg/153 mg?

SPAQ-Co Dispersible Tablets 500 mg/25 mg/153 mg contains Amodiaquine (Amodiaquine Hydrochloride); Sulfadoxine; Pyrimethamine (153 mg; 500 mg; 25 mg), as dispersible tablet, according to its NAFDAC registration record.

Is SPAQ-Co Dispersible Tablets 500 mg/25 mg/153 mg registered with NAFDAC?

Yes. SPAQ-Co Dispersible Tablets 500 mg/25 mg/153 mg is listed on the NAFDAC register under registration number B4-6482, and its registration is active as of 6 November 2026.

Has SPAQ-Co Dispersible Tablets 500 mg/25 mg/153 mg been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches SPAQ-Co Dispersible Tablets 500 mg/25 mg/153 mg in our automatically synced alert list.

How can I check that my pack of SPAQ-Co Dispersible Tablets 500 mg/25 mg/153 mg is genuine?

Run a free authenticity scan with the NAFDAC number B4-6482, 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 RxVerify users, not medical advice. Report side effects to your doctor and to NAFDAC.