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Eprostol 25 Tablet

NAFDAC Reg. No. A4-5420 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Eprostol 25 Tablet
NAFDAC number
A4-5420
Active ingredient
Misoprostol
Strength
25 mcg
Form
Vaginal tablet
Pack size
1 x 10's
Manufacturer
Not listed
Applicant (holder)
Zolon Healthcare Limited
Approved
30 Jun 2026
Status
Inactive View on NAFDAC ↗
Registration valid to
29 Jun 2031
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Eprostol 25 Tablet is on the NAFDAC register with an active registration (A4-5420). 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 Eprostol 25 Tablet

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 Eprostol 25 Tablet

What is in Eprostol 25 Tablet?

Eprostol 25 Tablet contains Misoprostol (25 mcg), as vaginal tablet, according to its NAFDAC registration record.

Is Eprostol 25 Tablet registered with NAFDAC?

Yes. Eprostol 25 Tablet is listed on the NAFDAC register under registration number A4-5420, and its registration is active as of 28 October 2026.

Has Eprostol 25 Tablet been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Eprostol 25 Tablet in our automatically synced alert list.

How can I check that my pack of Eprostol 25 Tablet is genuine?

Run a free authenticity scan with the NAFDAC number A4-5420, 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.