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Loratadine Tablets BP 10 mg

NAFDAC Reg. No. B4-9972 · Drug

Registered with NAFDAC — registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
Loratadine Tablets BP 10 mg
NAFDAC number
B4-9972
Active ingredient
Loratadine
Strength
10 mg
Form
Tablet
Pack size
10 x 10's (in Alu-PVC blisters)
Manufacturer
Not listed
Applicant (holder)
Priya Pharmaceutical Nig Ltd
Approved
25 Sep 2024
Status
Active View on NAFDAC ↗
Registration valid to
24 Sep 2029
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • 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.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. Not medical advice — always follow your doctor or pharmacist.

What Loratadine Tablets BP 10 mg 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 Loratadine Tablets BP 10 mg

Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.

3 free checks left today · no signup Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

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 5 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.

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.)

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