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AVI IBD Inter Live Vaccine

NAFDAC Reg. No. A6-0548 · Drug

Registered with NAFDAC. Registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
AVI IBD Inter Live Vaccine
NAFDAC number
A6-0548
Active ingredient
Avian infectious bursal (gumboro) disease vaccine, Live
Strength
see Composition
Form
Freeze-dried powder for suspension
Pack size
20 x 1000 doses (in vials)
Manufacturer
Not listed
Applicant (holder)
Vetilog Pharma Nigeria Limited
Approved
18 Dec 2024
Status
Active View on NAFDAC ↗
Registration valid to
17 Dec 2029
WHO alerts
None found
Community reports
None
Times checked
0

About the medicine: Avian infectious bursal: uses, dosage and brands worldwide

What we found

  • AVI IBD Inter Live Vaccine is on the NAFDAC register with an active registration (A6-0548). 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.

How to use AVI IBD Inter Live Vaccine

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

Temporarily relieves symptoms of runny nose, fever & cough.**

How to take it and how often

Adults & children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.

Warnings

IF PREGNANT OR BREAST-FEEDING , ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. Do not use if TAMPER EVIDENT seal is broken or missing.

How to store it

Keep out of reach of children.

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2025-12-18.

Label for AVI IBD Inter Live Vaccine, the active ingredient registered with NAFDAC.

NAFDAC recall & alert notices

Public Alert No. 35/2025 – Substandard batches of Annmox (Amoxicillin suspensions 125mg/5ml) and Jawamox (Amoxicillin suspension 125mg/5ml) manufactured by Jawa International Ltd due to low Active Pharmaceutical Ingredient (API) content22 Oct 2025 · nafdac.gov.ngThe National Agency for Food and Drugs Administration and Control (NAFDAC) is notifying the public about the mop up of batches of confirmed substandard Annmox (Batch 360M) and Jawamox (Batch 4231M & 4290M) Suspensions.The products failed laboratory analysis due to low Active Pharmaceutical Ingredient (API) content.The …Public Alert No. 032/2024 – Singapore to Ban Formaldehyde in Interior Paints over health concerns by 202622 Aug 2024 · nafdac.gov.ngThe National Agency for Food and Drugs Administration and Control (NAFDAC) is notifying the public that Singapore’s National Environment Agency (NEA) is banning the sale of indoor paints containing formaldehyde from 1 January 2026.To ensure compliance, paint manufacturers and importers will be mandated to submit test r…Public Alert No: 027/2022 – Adulterated Lots of Japata Alcoholic Bitters 100 ml (all variants) produced by Chigodson International Company Limited, Lagos10 May 2022 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC) is alerting the general public about adulterated lots of Japata Alcoholic Bitters 100 ml (all variants) produced by Chigodson International Company Limited, No. 30 Edegbami Offor Street, off Destiny Bus Stop, Isheri-Oshun Street, Alimosho LGA, …Public Alert No: 023/2020-Recall Of Winter Melon Strips Due To Excessive Levels Of Sulphur Dioxide27 Oct 2020 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC)  has been informed that the Singapore Food Agency (SFA) has detected sulphur dioxide, an allergen, in samples of winter melon strips at levels exceeding the maximum limit for sulphur dioxide as stated in the Singapore Food Regulations. 2 SFA ha…

Compare the brands and batch numbers in these notices with your pack, or enter your batch number above.

Check your pack of AVI IBD Inter Live Vaccine

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

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3 free checks left today Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About AVI IBD Inter Live Vaccine

What is in AVI IBD Inter Live Vaccine?

AVI IBD Inter Live Vaccine contains Avian infectious bursal (gumboro) disease vaccine, Live (see Composition), as freeze-dried powder for suspension, according to its NAFDAC registration record.

Is AVI IBD Inter Live Vaccine registered with NAFDAC?

Yes. AVI IBD Inter Live Vaccine is listed on the NAFDAC register under registration number A6-0548, and its registration is active as of 5 November 2026.

Has AVI IBD Inter Live Vaccine been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches AVI IBD Inter Live Vaccine in our automatically synced alert list.

How can I check that my pack of AVI IBD Inter Live Vaccine is genuine?

Run a free authenticity scan with the NAFDAC number A6-0548, 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.

How do I take AVI IBD Inter Live Vaccine?

Follow your prescription or the leaflet in your pack. The official label says: Adults & children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.…

What is AVI IBD Inter Live Vaccine used for?

Temporarily relieves symptoms of runny nose, fever & cough.** (Summarised from the official U.S. FDA label for AVI IBD Inter Live Vaccine. Always follow your doctor or pharmacist.)

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