VETOFLOK LA, 100 mg/mL, otopina za injekciju, za goveda
VETOFLOK LA, 100 mg/mL, otopina za injekciju, za goveda
Not authorised
- Enrofloxacin
Product identification
Medicine name:
VETOFLOK LA, 100 mg/mL, otopina za injekciju, za goveda
Active substance:
- Enrofloxacin
Target species:
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Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Enrofloxacin100.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
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Solution for injection
Withdrawal period by route of administration:
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Subcutaneous use
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Cattle
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Meat and offal14day
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Milk5day
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Milk120hourMlijeko se može koristiti nakon što protekne 120 sati od aplikacije VMP-a, tj. poslije desete mužnje uz uvjet da se krave muze 2 x na dan
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Revoked
Authorised in:
-
Croatia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (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-322-05/17-01/354
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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Croatian (PDF)
Published on: 11/02/2022