AVITUBAL - 28 000 injekčný roztok, tuberkulín aviárny – 28 000 IU/ml
AVITUBAL - 28 000 injekčný roztok, tuberkulín aviárny – 28 000 IU/ml
Authorised
- Mycobacterium avium, subsp. avium, strain D4ER, avian tuberculin purified protein derivative
Product identification
Medicine name:
AVITUBAL - 28 000 injekčný roztok, tuberkulín aviárny – 28 000 IU/ml
Active substance:
- Mycobacterium avium, subsp. avium, strain D4ER, avian tuberculin purified protein derivative
Target species:
-
Chicken
-
Cattle
-
Pig
Route of administration:
-
Intradermal use
Product details
Active substance and strength:
-
Mycobacterium avium, subsp. avium, strain D4ER, avian tuberculin purified protein derivative28000.00international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intradermal use
- Chicken
-
All relevant tissues0day
-
- Cattle
-
All relevant tissues0day
-
- Pig
-
All relevant tissues0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QV04CF01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Package description:
- Available only in Slovak
- Available only in Slovak
- Available only in Slovak
- Available only in Slovak
- Available only in Slovak
- Available only in Slovak
- Available only in Slovak
- Available only in Slovak
- Available only in Slovak
- Available only in Slovak
- Available only in Slovak
- Available only in Slovak
- Available only in Slovak
- Available only in Slovak
- Available only in Slovak
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:
- Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 97/051/03-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Slovak (PDF)
Published on: 3/01/2022
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