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Gida / Rijista a Najeriya / Xential Ferrous Sulphate Tablets

Xential Ferrous Sulphate Tablets

NAFDAC Reg. A'a. A11-100669 · Magungunan miyagun ƙwayoyi

Rijista tare da NAFDAC. Rijista mai aikiAs of 5 November 2026 · synced automatically from official sources.
Product
Xential Ferrous Sulphate Tablets
NAFDAC number
A11-100669
Active ingredient
Ferrous sulfate
Strength
200 mg
Form
Tablet
Pack size
1 x 1000's (in a jar)
Manufacturer
Not listed
Applicant (holder)
Xential Pharmaceuticals Nig Ltd
Approved
28 Feb 2024
Status
Active View on NAFDAC ↗
Registration valid to
27 Feb 2029
WHO alerts
None found
Community reports
None
Times checked
0

About the medicine: Ferrous sulfate: uses, dosage and brands worldwide

What we found

  • Xential Ferrous Sulphate Tablets is on the NAFDAC register with an active registration (A11-100669). 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.

How to use Xential Ferrous Sulphate Tablets

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

See symptoms on front panel. Relieves hot flashes with headaches *

How to take it and how often

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

Possible side effects

Symptoms persist for more than 3 days or worsen.

Pregnancy and breastfeeding

If pregnant or breast-feeding, ask a health professional before use.

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2025-07-21.

Label for ferrous sulfate, the active ingredient registered with NAFDAC.

Check your pack of Xential Ferrous Sulphate Tablets

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

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Xential Ferrous Sulphate Tablets

What is in Xential Ferrous Sulphate Tablets?

Xential Ferrous Sulphate Tablets contains Ferrous sulfate (200 mg), as tablet, according to its NAFDAC registration record.

Is Xential Ferrous Sulphate Tablets registered with NAFDAC?

Yes. Xential Ferrous Sulphate Tablets is listed on the NAFDAC register under registration number A11-100669, and its registration is active as of 5 November 2026.

Has Xential Ferrous Sulphate Tablets been flagged as fake or recalled?

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

How can I check that my pack of Xential Ferrous Sulphate Tablets is genuine?

Run a free authenticity scan with the NAFDAC number A11-100669, 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.

How do I take Xential Ferrous Sulphate Tablets?

Follow your prescription or the leaflet in your pack. The official label says: Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.…

What is Xential Ferrous Sulphate Tablets used for?

See symptoms on front panel. Relieves hot flashes with headaches * (Summarised from the official U.S. FDA label for ferrous sulfate. Always follow your doctor or pharmacist.)

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Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.