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Mefspas Tablet

NAFDAC REG NO: A4-100899 Médicament

Enregistré auprès de NAFDAC. Enregistrement actifAs of 6 November 2026 · synced automatically from official sources.
Produit
Mefspas Tablet
Numéro NAFDAC
A4-100899
Principe actif
Drotaverine Hydrochloride
Dosage
80 mg
Forme
Tablet
Conditionnement
1 x 10's (in Alu-Alu blister)
Fabricant
Non répertorié
Déposant / Titulaire :
Ncure Healthcare Ltd
Approuvé
27 Jun 2024
Statut
Actif Vue sur NAFDAC ↗
Enregistrement valable jusqu'au
26 Jun 2029
Alertes OMS
Non trouvé
Community reports
None
Times checked
0

What we found

  • Mefspas Tablet is on the NAFDAC register with an active registration (A4-100899). 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 Mefspas Tablet

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

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Encore 3 vérifications gratuites aujourd'hui Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Mefspas Tablet

What is in Mefspas Tablet?

Mefspas Tablet contains Drotaverine Hydrochloride (80 mg), as tablet, according to its NAFDAC registration record.

Is Mefspas Tablet registered with NAFDAC?

Yes. Mefspas Tablet is listed on the NAFDAC register under registration number A4-100899, and its registration is active as of 6 November 2026.

Has Mefspas Tablet been flagged as fake or recalled?

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

How can I check that my pack of Mefspas Tablet is genuine?

Run a free authenticity scan with the NAFDAC number A4-100899, 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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