Proviron 25 mg Tablet — NAFDAC 04-1300: Is It Genuine? Uses, Alerts

Produkt-: Proviron 25 mg Tablet
NAFDAC-Nummer: 04-1300
Wirkstoff: Mesterolone
Stärke: 25 mg
Form: Tablet
VPE:: 2 x 10's (in Alu/PVC blisters)
Hersteller: Nicht aufgeführt
Applicant (holder): Bayer Nigeria Limited
Approved: 23 Feb 2023
Status: Active View on NAFDAC ↗
Registration valid to: 22 Feb 2028
WER WARNT: None found
Community reports: None
Times checked: 0

About the medicine: Mesterolone: uses, dosage and brands worldwide

What we found

Proviron 25 mg Tablet is on the NAFDAC register with an active registration (04-1300). 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 Proviron 25 mg Tablet

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

3 free checks left today Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Proviron 25 mg Tablet

What is in Proviron 25 mg Tablet?

Proviron 25 mg Tablet contains Mesterolone (25 mg), as tablet, according to its NAFDAC registration record.

Is Proviron 25 mg Tablet registered with NAFDAC?

Yes. Proviron 25 mg Tablet is listed on the NAFDAC register under registration number 04-1300, and its registration is active as of 6 November 2026.

Has Proviron 25 mg Tablet been flagged as fake or recalled?

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

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

Run a free authenticity scan with the NAFDAC number 04-1300, 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.