Verifying…
Home / Drug A–Z / Xonadine 120 mg

Xonadine 120 mg

NAFDAC Reg. No. A4-8122 · Drug

Registered with NAFDAC. Registration activeAs of 27 October 2026 · synced automatically from official sources.
Product
Xonadine 120 mg
NAFDAC number
A4-8122
Active ingredient
Fexofenadine Hydrochloride
Strength
120 mg
Form
Capsule
Pack size
1 x 10's
Manufacturer
Not listed
Applicant (holder)
Micro Nova Pharmaceuticals Ind Ltd
Approved
3 Aug 2021
Status
Inactive View on NAFDAC ↗
Registration valid to
2 Aug 2026
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Xonadine 120 mg is on the NAFDAC register with an active registration (A4-8122). 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 Xonadine 120 mg is used for

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

What it is used for

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

Purpose

Antihistamine

Warnings

Do not use if you ever had an allergic reaction to this product or any of its ingredients Ask a doctor before using if you have kidney disease. Your doctor should determine if you need a different dose. When using this product do not take more than directed do not take at the same time as aluminum or magnesium antacids do not take with fruit juices (see Directions) 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 healthcare professional before use. Keep out of reach of children . In case of overdose, get medical help or contact a Poison Control Center right away.

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

Check your pack of Xonadine 120 mg

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 Xonadine 120 mg

What is in Xonadine 120 mg?

Xonadine 120 mg contains Fexofenadine Hydrochloride (120 mg), as capsule, according to its NAFDAC registration record.

Is Xonadine 120 mg registered with NAFDAC?

Yes. Xonadine 120 mg is listed on the NAFDAC register under registration number A4-8122, and its registration is active as of 27 October 2026.

Has Xonadine 120 mg been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Xonadine 120 mg in our automatically synced alert list.

How can I check that my pack of Xonadine 120 mg is genuine?

Run a free authenticity scan with the NAFDAC number A4-8122, 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 Xonadine 120 mg used for?

temporarily relieves these symptoms due to hay fever or other respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat (Summarised from the official U.S. FDA label for fexofenadine hydrochloride. Always follow your doctor or pharmacist.)

Patient reviews

–No reviews yet
5★
0
4★
0
3★
0
2★
0
1★
0
Have you used Xonadine 120 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.