Zycort Tablet — NAFDAC A4-9740: Is It Genuine? Uses, Alerts

Producto: Zycort Tablet
Número NAFDAC: A4-9740
Principio activo: Prednisolone
Dosis: 5 mg
Forma: Tablet
Tamaño del envase: 10 x 10's
Fabricante: No Constan
Solicitante (titular): Zadip Pharma Nig Ltd
Approved: 7 May 2021
Estado: Inactive Ver en NAFDAC ↗
Registro válido hasta: 6 May 2026
Alertas de la OMS: No se ha encontrado ninguno
Informes de la comunidad: Ninguno
Tiempos comprobados: 0

Pero sobre el medicamento, Prednisolone: uses, dosage and brands worldwide

Lo que encontramos

Zycort Tablet is on the NAFDAC register with an active registration (A4-9740). 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.

Generado automáticamente a partir del registro NAFDAC, QUIÉN alerta y los datos de la comunidad a partir de hoy. Este no es un consejo médico. Siga siempre a su médico o farmacéutico.

Check your pack of Zycort Tablet

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

Te quedan 3 verificaciones gratis hoy Fuentes oficiales: FDA de EE. UU. · EMA (UE) · NAFDAC · alertas de la OMS

About Zycort Tablet

What is in Zycort Tablet?

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

Is Zycort Tablet registered with NAFDAC?

Yes. Zycort Tablet is listed on the NAFDAC register under registration number A4-9740, and its registration is active as of 29 October 2026.

Has Zycort Tablet been flagged as fake or recalled?

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

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

Run a free authenticity scan with the NAFDAC number A4-9740, 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.