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Accueil / Enregistré au Nigeria / Loratidine Tablet

Loratidine Tablet

NAFDAC REG NO: B4-0483 Médicament

Enregistré auprès de NAFDAC. Enregistrement actifAs of 6 November 2026 · synced automatically from official sources.
Produit
Loratidine Tablet
Numéro NAFDAC
B4-0483
Principe actif
Loratadine
Dosage
10 mg
Forme
Tablet
Conditionnement
10 x 10's
Fabricant
Non répertorié
Déposant / Titulaire :
Azmu Pharmaceuticals Limited
Approuvé
24 Jun 2021
Statut
Inactive Vue sur NAFDAC ↗
Enregistrement valable jusqu'au
23 Jun 2026
Alertes OMS
Non trouvé
Community reports
None
Times checked
0

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

What we found

  • Loratidine Tablet is on the NAFDAC register with an active registration (B4-0483). 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 Loratidine Tablet

Ce que dit la notice officielle. Si un médecin vous l'a prescrit, suivez l'ordonnance. La notice de votre boîte prime si elle est différente.

Pour qui

Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose • itchy, watery eyes • sneezing • itching of the nose or throat

Comment le prendre et à quelle fréquence
  • Adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours
  • Children under 6 years of age
  • Ask a doctor consumers with liver or kidney disease
  • Ask a doctor
While you are taking it
  • Do not take more than directed
  • Taking more than directed may cause drowsiness
Talk to a doctor first if
  • Liver or kidney disease
  • Your doctor should determine if you need a different dose
Warnings

Do not use if you have ever had an allergic reaction to this product or any of its ingredients Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose. When using this product do not take more than directed. Taking more than directed may cause drowsiness. Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Effets secondaires possibles

An allergic reaction to this product occurs. Seek medical help right away.

Pregnancy and breastfeeding

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

How to store it

• do not use if printed foil under cap is broken or missing • store between 20 ° to 25 ° C (68 ° to 77 ° F) Keep out of reach of children.

En cas d'oubli

Prenez-le dès que vous y pensez, sauf s'il est presque l'heure de la dose suivante. Dans ce cas, sautez la dose oubliée. Ne prenez jamais deux doses à la fois pour compenser. Vérifiez votre notice, certains médicaments font exception.

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 2026-02-25.

Label for loratadine, the active ingredient registered with NAFDAC.

Check your pack of Loratidine Tablet

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

Ou prenez la boîte en photo
Encore 3 vérifications gratuites aujourd'hui Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Loratidine Tablet

What is in Loratidine Tablet?

Loratidine Tablet contains Loratadine (10 mg), as tablet, according to its NAFDAC registration record.

Is Loratidine Tablet registered with NAFDAC?

Yes. Loratidine Tablet is listed on the NAFDAC register under registration number B4-0483, and its registration is active as of 6 November 2026.

Has Loratidine Tablet been flagged as fake or recalled?

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

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

Run a free authenticity scan with the NAFDAC number B4-0483, 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 Loratidine Tablet?

Follow your prescription or the leaflet in your pack. The official label says: adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor…

What is Loratidine Tablet used for?

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose • itchy, watery eyes • sneezing • itching of the nose or throat (Summarised from the official U.S. FDA label for loratadine. 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.