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Início / Registado na Nigéria / Agesulf Ferrous Sulphate Tablets

Agesulf Ferrous Sulphate Tablets

NAFDAC Reg. No. A11-100759 · Drug

Registered with NAFDAC. Registration activeAs of 2 November 2026 · synced automatically from official sources.
Product
Agesulf Ferrous Sulphate Tablets
Número NAFDAC
A11-100759
Princípio ativo
Ferrous sulfate
Dosagem
200 mg
Forma
Tablet
Tamanho da embalagem
1 x 1000's
Manufacturer
Not listed
Applicant (holder)
Agelex Pharmaceuticals Limited
Approved
28 Aug 2024
Situação
Active View on NAFDAC ↗
Registro válido até
27 Aug 2029
Alertas da OMS
None found
Community reports
None
Times checked
0

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

What we found

  • Agesulf Ferrous Sulphate Tablets is on the NAFDAC register with an active registration (A11-100759). 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 Agesulf Ferrous Sulphate Tablets

O que diz a bula oficial. Se um médico receitou, siga a receita. Se a bula da sua caixa for diferente, vale a da sua caixa.

Para quem é

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

Como tomar e com que frequência

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.

Possíveis efeitos colaterais

Symptoms persist for more than 3 days or worsen.

Pregnancy and breastfeeding

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

Se esquecer uma dose

Tome assim que lembrar, a menos que esteja quase na hora da próxima dose. Nesse caso, pule a dose esquecida. Nunca tome duas doses de uma vez para compensar. Confira a bula, pois alguns medicamentos são diferentes.

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 Agesulf Ferrous Sulphate Tablets

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

Ou tire fotos da caixa
Restam 3 verificações grátis hoje Fontes oficiais: FDA dos EUA · EMA (UE) · NAFDAC · alertas da OMS

About Agesulf Ferrous Sulphate Tablets

What is in Agesulf Ferrous Sulphate Tablets?

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

Is Agesulf Ferrous Sulphate Tablets registered with NAFDAC?

Yes. Agesulf Ferrous Sulphate Tablets is listed on the NAFDAC register under registration number A11-100759, and its registration is active as of 2 November 2026.

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

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

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

Run a free authenticity scan with the NAFDAC number A11-100759, 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 Agesulf 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 Agesulf 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.