Veterinary Medicines

TAbic IB VAR206, effervescent tablets for suspension for chickens

Authorised
  • Avian infectious bronchitis virus, strain 2-06, Live
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Product identification

Medicine name:
TAbic IB VAR206, effervescent tablets for suspension for chickens
TAbic IB VAR206, šumeče tablete za suspenzijo za piščance
Active substance:
  • Avian infectious bronchitis virus, strain 2-06, Live
Target species:
  • Chicken (hen)
Route of administration:
  • Nebulisation use

Product details

Active substance and strength:
  • Avian infectious bronchitis virus, strain 2-06, Live
Pharmaceutical form:
  • Effervescent tablet
Withdrawal period by route of administration:
  • Nebulisation use
    • Chicken (hen)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AD07
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovenia
Package description:
  • Available only in Slovenian
  • Available only in Slovenian
  • Available only in Slovenian
  • Available only in Slovenian
  • Available only in Slovenian
  • Available only in Slovenian
  • Available only in Slovenian
  • Available only in Slovenian
  • Available only in Slovenian
  • Available only in Slovenian
  • Available only in Slovenian
  • Available only in Slovenian
  • Tablets (1500 doses) are packed in Aluminium – Aluminium blisters: Alum Soft Silver (PVC/PVDC) – Alum Silver (PVC). Each blister contains 10 tablets. Cardboard box contains 1 blister.
  • Tablets (3000 doses) are packed in Aluminium – Aluminium blisters: Alum Soft Silver (PVC/PVDC) – Alum Silver (PVC). Each blister contains 10 tablets. Cardboard box contains 1 blister.
  • Tablets (3500 doses) are packed in Aluminium – Aluminium blisters: Alum Soft Silver (PVC/PVDC) – Alum Silver (PVC). Each blister contains 10 tablets. Cardboard box contains 1 blister.
  • Tablets (4000 doses) are packed in Aluminium – Aluminium blisters: Alum Soft Silver (PVC/PVDC) – Alum Silver (PVC). Each blister contains 10 tablets. Cardboard box contains 1 blister.
  • Tablets (4500 doses) are packed in Aluminium – Aluminium blisters: Alum Soft Silver (PVC/PVDC) – Alum Silver (PVC). Each blister contains 10 tablets. Cardboard box contains 1 blister.
  • Tablets (1500 doses) are packed in Aluminium – Aluminium blisters: Alum Soft Silver (PVC/PVDC) – Alum Silver (PVC). Each blister contains 10 tablets. Cardboard box contains 2 blisters.
  • Tablets (3000 doses) are packed in Aluminium – Aluminium blisters: Alum Soft Silver (PVC/PVDC) – Alum Silver (PVC). Each blister contains 10 tablets. Cardboard box contains 2 blisters.
  • Tablets (3500 doses) are packed in Aluminium – Aluminium blisters: Alum Soft Silver (PVC/PVDC) – Alum Silver (PVC). Each blister contains 10 tablets. Cardboard box contains 2 blisters.
  • Tablets (4000 doses) are packed in Aluminium – Aluminium blisters: Alum Soft Silver (PVC/PVDC) – Alum Silver (PVC). Each blister contains 10 tablets. Cardboard box contains 2 blisters.
  • Tablets (4500 doses) are packed in Aluminium – Aluminium blisters: Alum Soft Silver (PVC/PVDC) – Alum Silver (PVC). Each blister contains 10 tablets. Cardboard box contains 2 blisters.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Phibro Animal Health (Poland) Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Synoptis Industrial Sp. z o.o.
Responsible authority:
  • Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
  • MR/V/0682/001
Date of authorisation status change:
Reference member state:
  • Poland
Procedure number:
  • PL/V/0109/001/MR
Concerned member states:
  • Bulgaria
  • Czechia
  • Latvia
  • Lithuania
  • Romania
  • Slovakia
  • Slovenia

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 27/01/2025
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 27/01/2025
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 27/01/2025
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Combined File of all Documents

English (PDF)
Published on: 7/02/2024
Updated on: 8/02/2024
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