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Replek Loratadine Syrup

NAFDAC Reg. No. C4-1259 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Replek Loratadine Syrup
NAFDAC number
C4-1259
Active ingredient
Loratadine
Strength
5 mg/5 mL
Form
Syrup
Manufacturer
Not listed
Applicant (holder)
Bio-Generics Nigeria Limited
Approved
10 Nov 2020
Status
Inactive View on NAFDAC ↗
Registration valid to
9 Nov 2025
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Replek Loratadine Syrup is on the NAFDAC register with an active registration (C4-1259). 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.

What Replek Loratadine Syrup is used for

From the official U.S. FDA label for loratadine, the active ingredient registered with NAFDAC.

What it is 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

Purpose

Antihistamine

Possible side effects

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

Do not use if

if you have ever had an allergic reaction to this product or any of its ingredients

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)

Pregnancy & breastfeeding

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

Storage

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

General information only, not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

Check your pack of Replek Loratadine Syrup

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

3 free checks left today Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Replek Loratadine Syrup

What is in Replek Loratadine Syrup?

Replek Loratadine Syrup contains Loratadine (5 mg/5 mL), as syrup, according to its NAFDAC registration record.

Is Replek Loratadine Syrup registered with NAFDAC?

Yes. Replek Loratadine Syrup is listed on the NAFDAC register under registration number C4-1259, and its registration is active as of 28 October 2026.

Has Replek Loratadine Syrup been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Replek Loratadine Syrup in our automatically synced alert list.

How can I check that my pack of Replek Loratadine Syrup is genuine?

Run a free authenticity scan with the NAFDAC number C4-1259, 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.

What is Replek Loratadine Syrup 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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