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Krishat Loratadine Tablets_

NAFDAC Reg. No. A11-100909 · Drug

Registered with NAFDAC — registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
Krishat Loratadine Tablets_
NAFDAC number
A11-100909
Active ingredient
Loratadine
Strength
10 mg
Form
Tablet
Pack size
10 x 10's (in Alu-PVC blisters)
Manufacturer
Not listed
Applicant (holder)
Krishat Pharma Industries Limited
Approved
25 Jun 2025
Status
Active View on NAFDAC ↗
Registration valid to
24 Jun 2030
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Krishat Loratadine Tablets_ is on the NAFDAC register with an active registration (A11-100909). 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 Krishat Loratadine Tablets_ 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 Krishat Loratadine Tablets_

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 Krishat Loratadine Tablets_

What is in Krishat Loratadine Tablets_?

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

Is Krishat Loratadine Tablets_ registered with NAFDAC?

Yes. Krishat Loratadine Tablets_ is listed on the NAFDAC register under registration number A11-100909, and its registration is active as of 5 November 2026.

Has Krishat Loratadine Tablets_ been flagged as fake or recalled?

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

How can I check that my pack of Krishat Loratadine Tablets_ is genuine?

Run a free authenticity scan with the NAFDAC number A11-100909, 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 Krishat Loratadine Tablets_ 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.