BOVINI TUBERKULIN PPD 28 000 i.j., otopina za injekciju za goveda i svinje
BOVINI TUBERKULIN PPD 28 000 i.j., otopina za injekciju za goveda i svinje
Authorised
- Mycobacterium bovis, strain AN5, bovine tuberculin purified protein derivative
Product identification
Medicine name:
BOVINI TUBERKULIN PPD 28 000 i.j., otopina za injekciju za goveda i svinje
Active substance:
- Mycobacterium bovis, strain AN5, bovine tuberculin purified protein derivative
Target species:
-
Cattle
-
Pig
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Mycobacterium bovis, strain AN5, bovine tuberculin purified protein derivative28000.00/international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Pig
-
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:
-
Croatia
Package description:
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
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:
- Genera d.d.
Marketing authorisation date:
Manufacturing sites for batch release:
- Genera d.d.
Responsible authority:
- Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
- UP/I-322-05/20-01/284
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
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in another language below.
Croatian (PDF)
Published on: 20/05/2025