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Duspatalin Tablets

NAFDAC Reg. No. 04-1302 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Duspatalin Tablets
NAFDAC number
04-1302
Active ingredient
Mebeverine Hydrochloride
Strength
135 mg
Form
Tablet
Pack size
1 x 50's
Manufacturer
Not listed
Applicant (holder)
Phillips Pharmaceuticals (Nigeria) Limited
Approved
28 Jan 2021
Status
Inactive View on NAFDAC ↗
Registration valid to
27 Jan 2026
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Duspatalin Tablets is on the NAFDAC register with an active registration (04-1302). 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 Duspatalin Tablets

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

3 free checks left today Official sources: NAFDAC · WHO · U.S. FDA · Health Canada · NLM

About Duspatalin Tablets

What is in Duspatalin Tablets?

Duspatalin Tablets contains Mebeverine Hydrochloride (135 mg), as tablet, according to its NAFDAC registration record.

Is Duspatalin Tablets registered with NAFDAC?

Yes. Duspatalin Tablets is listed on the NAFDAC register under registration number 04-1302, and its registration is active as of 28 October 2026.

Has Duspatalin Tablets been flagged as fake or recalled?

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

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

Run a free authenticity scan with the NAFDAC number 04-1302, 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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