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Everdrex Tablets

NAFDAC Reg. No. A11-100339 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Everdrex Tablets
NAFDAC number
A11-100339
Active ingredient
Diclofenac Potassium
Strength
50 mg
Form
Tablet
Manufacturer
Not listed
Applicant (holder)
Evergreen Morning Star Pharmaceutical Ind. Ltd
Approved
16 Dec 2021
Status
Active View on NAFDAC ↗
Registration valid to
15 Dec 2026
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Everdrex Tablets is on the NAFDAC register with an active registration (A11-100339). 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 Everdrex 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 Everdrex Tablets

What is in Everdrex Tablets?

Everdrex Tablets contains Diclofenac Potassium (50 mg), as tablet, according to its NAFDAC registration record.

Is Everdrex Tablets registered with NAFDAC?

Yes. Everdrex Tablets is listed on the NAFDAC register under registration number A11-100339, and its registration is active as of 28 October 2026.

Has Everdrex Tablets been flagged as fake or recalled?

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

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

Run a free authenticity scan with the NAFDAC number A11-100339, 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.