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Pulmicort Nebulising Suspension

NAFDAC Reg. No. A4-6468 · Drug

Registered with NAFDAC — registration activeAs of 6 November 2026 · synced automatically from official sources.
Product
Pulmicort Nebulising Suspension
NAFDAC number
A4-6468
Active ingredient
Budesonide
Strength
0.25 mg/mL
Form
Suspension
Pack size
20 x 2 mL
Manufacturer
Not listed
Applicant (holder)
AstraZeneca Nigeria Limited
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

RxVerify commentary

  • Pulmicort Nebulising Suspension is on the NAFDAC register with an active registration (A4-6468). 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 Pulmicort Nebulising Suspension is used for

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

What it is used for

s Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • runny nose • itchy nose • sneezing

Purpose

Nasal allergy symptom reliever

Possible side effects

you have, or come into contact with someone who has, chickenpox, measles or tuberculosis you have or develop symptoms of an infection such as persistent fever you have any change in vision you have severe or frequent nosebleeds

Do not use if

in children under 6 years of age if you have ever had an allergic reaction to any of the ingredients

Warnings

Do not use in children under 6 years of age if you have ever had an allergic reaction to any of the ingredients Ask a doctor before use if you have had recent nose ulcers or nose surgery have had a nose injury that has not healed are using a steroid medicine for asthma, allergies or skin rash have an eye infection have or had glaucoma or cataracts When using this product the growth rate of some children may be slower some symptoms may get better on the first day of treatment. It may take up to two weeks of daily use to feel the most symptom relief. …

Pregnancy & breastfeeding

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

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

Check your pack of Pulmicort Nebulising Suspension

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 Pulmicort Nebulising Suspension

What is in Pulmicort Nebulising Suspension?

Pulmicort Nebulising Suspension contains Budesonide (0.25 mg/mL), as suspension, according to its NAFDAC registration record.

Is Pulmicort Nebulising Suspension registered with NAFDAC?

Yes. Pulmicort Nebulising Suspension is listed on the NAFDAC register under registration number A4-6468, and its registration is active as of 6 November 2026.

Has Pulmicort Nebulising Suspension been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Pulmicort Nebulising Suspension in our automatically synced alert list.

How can I check that my pack of Pulmicort Nebulising Suspension is genuine?

Run a free authenticity scan with the NAFDAC number A4-6468, 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 Pulmicort Nebulising Suspension used for?

s Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • runny nose • itchy nose • sneezing (Summarised from the official U.S. FDA label for budesonide. Always follow your doctor or pharmacist.)

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