Verificando…
Traducido automáticamente. Dosis y advertencias: consulta el original en inglés. Leer en inglés
Inicio / Registrado en Nigeria / Loratadine Tablets BP 10 mg

Loratadine Tablets BP 10 mg

NAFDAC Reg. No. B4-9972 Estupefaciente

Registrado en NAFDAC. Registro activoAs of 4 November 2026 · synced automatically from official sources.
Producto
Loratadine Tablets BP 10 mg
Número NAFDAC
B4-9972
Principio activo
Loratadine
Dosis
10 mg
Forma
Tablet
Tamaño del envase
10 x 10's (in Alu-PVC blisters)
Fabricante
No Constan
Solicitante (titular)
Priya Pharmaceutical Nig Ltd
Approved
25 Sep 2024
Estado
Activo Ver en NAFDAC ↗
Registro válido hasta
24 Sep 2029
Alertas de la OMS
No se ha encontrado ninguno
Informes de la comunidad
Ninguno
Tiempos comprobados
0

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

Lo que encontramos

  • Loratadine Tablets BP 10 mg is on the NAFDAC register with an active registration (B4-9972). 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.

How to use Loratadine Tablets BP 10 mg

Lo que dice el prospecto oficial. Si te lo recetó un médico, sigue la receta. Si el prospecto de tu caja es distinto, manda el de tu caja.

Para quién es

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

Cómo tomarlo y con qué frecuencia
  • 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)

Posibles efectos secundarios

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.

Si olvidas una dosis

Tómala en cuanto te acuerdes, salvo que falte poco para la siguiente. En ese caso, sáltate la olvidada. Nunca tomes dos dosis a la vez para compensar. Revisa tu prospecto, porque algunos medicamentos son distintos.

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 Loratadine Tablets BP 10 mg

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

O haz fotos de la caja
Te quedan 3 verificaciones gratis hoy Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Loratadine Tablets BP 10 mg

What is in Loratadine Tablets BP 10 mg?

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

Is Loratadine Tablets BP 10 mg registered with NAFDAC?

Yes. Loratadine Tablets BP 10 mg is listed on the NAFDAC register under registration number B4-9972, and its registration is active as of 4 November 2026.

Has Loratadine Tablets BP 10 mg been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Loratadine Tablets BP 10 mg in our automatically synced alert list.

How can I check that my pack of Loratadine Tablets BP 10 mg is genuine?

Run a free authenticity scan with the NAFDAC number B4-9972, 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 Loratadine Tablets BP 10 mg?

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 Loratadine Tablets BP 10 mg 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.)

Patient reviews

–No reviews yet
5★
0
4★
0
3★
0
2★
0
1★
0
Have you used Loratadine Tablets BP 10 mg? Share your experience to help other patients. Sign in to review

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