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Home / Drug A–Z / Predilin Tablets

Predilin Tablets

NAFDAC Reg. No. 04-9973 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Predilin Tablets
NAFDAC number
04-9973
Active ingredient
Prednisolone
Strength
5 mg
Form
Tablet
Pack size
10 x 10's (in PVC-Alu blisters)
Manufacturer
Not listed
Applicant (holder)
Geneith Pharmaceuticals Limited
Approved
30 Apr 2024
Status
Active View on NAFDAC ↗
Registration valid to
1 May 2029
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Predilin Tablets is on the NAFDAC register with an active registration (04-9973). 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 Predilin 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 Predilin Tablets

What is in Predilin Tablets?

Predilin Tablets contains Prednisolone (5 mg), as tablet, according to its NAFDAC registration record.

Is Predilin Tablets registered with NAFDAC?

Yes. Predilin Tablets is listed on the NAFDAC register under registration number 04-9973, and its registration is active as of 28 October 2026.

Has Predilin Tablets been flagged as fake or recalled?

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

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

Run a free authenticity scan with the NAFDAC number 04-9973, 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.