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Tofen Eye Drops

NAFDAC Reg. No. B4-8756 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Tofen Eye Drops
NAFDAC number
B4-8756
Active ingredient
Ketotifen (Ketotifen Fumarate)
Strength
0.345 mg
Form
Eye drops
Pack size
1 x 5 mL
Manufacturer
Not listed
Applicant (holder)
Pharmadeal Nigeria Limited
Approved
24 Jun 2021
Status
Inactive View on NAFDAC ↗
Registration valid to
23 Jun 2026
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Tofen Eye Drops is on the NAFDAC register with an active registration (B4-8756). 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 Tofen Eye Drops

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 Tofen Eye Drops

What is in Tofen Eye Drops?

Tofen Eye Drops contains Ketotifen (Ketotifen Fumarate) (0.345 mg), as eye drops, according to its NAFDAC registration record.

Is Tofen Eye Drops registered with NAFDAC?

Yes. Tofen Eye Drops is listed on the NAFDAC register under registration number B4-8756, and its registration is active as of 28 October 2026.

Has Tofen Eye Drops been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Tofen Eye Drops in our automatically synced alert list.

How can I check that my pack of Tofen Eye Drops is genuine?

Run a free authenticity scan with the NAFDAC number B4-8756, 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.