Avitubal 28000, 28000 IU Roztwór do wstrzykiwań
Avitubal 28000, 28000 IU Roztwór do wstrzykiwań
Authorised
- Mycobacterium avium, subsp. avium, strain D4ER, avian tuberculin protein derivative
Product identification
Medicine name:
Avitubal 28000, 28000 IU Roztwór do wstrzykiwań
Active substance:
- Mycobacterium avium, subsp. avium, strain D4ER, avian tuberculin protein derivative
Target species:
-
Turkey
-
Cattle
-
Pig
-
Chicken (hen)
Route of administration:
-
Intradermal use
Product details
Active substance and strength:
-
Mycobacterium avium, subsp. avium, strain D4ER, avian tuberculin protein derivative28000.00/international unit(s)1.00international unit(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intradermal use
-
Turkey
-
Meat and offal0day
-
-
Cattle
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
Chicken (hen)
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QV04CF01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Available in:
-
Poland
Package description:
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
- Available only in Polish
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:
- Grabikowski-Grabikowska Przedsiebiorstwo Produkcyjno-Handlowo-Uslugowe Inex Sp. j.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 2009
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 23/10/2024
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 23/10/2024
Labelling
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 23/10/2024