MARBOCYL 20 MG/ML SOLUTION FOR INJECTION FOR CATTLE AND PIGS
MARBOCYL 20 MG/ML SOLUTION FOR INJECTION FOR CATTLE AND PIGS
Authorised
- Marbofloxacin
Product identification
Medicine name:
MARBOCYL 20 MG/ML SOLUTION FOR INJECTION FOR CATTLE AND PIGS
MARBOCYL 2%
Active substance:
- Marbofloxacin
Target species:
-
Cattle (calf)
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
-
Intravenous use
Product details
Active substance and strength:
-
Marbofloxacin20.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle (calf)
-
Meat and offal6day
-
Milkno withdrawal periodThe veterinary medicinal product is not authorised for use in lactating animals producing milk for human consumption.
-
-
Pig
-
Meat and offal4day
-
-
-
Subcutaneous use
-
Cattle (calf)
-
Meat and offal6day
-
Milkno withdrawal periodThe veterinary medicinal product is not authorised for use in lactating animals producing milk for human consumption.
-
-
-
Intravenous use
-
Cattle (calf)
-
Meat and offal6day
-
Milkno withdrawal periodThe veterinary medicinal product is not authorised for use in lactating animals producing milk for human consumption.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA93
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Package description:
- Box of one vial of 10 ml
- Box of one vial of 250 ml
- Box of one vial of 100 ml
- Box of one vial of 50 ml
- Box of one vial of 20 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Vetoquinol S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Vetoquinol Biowet Sp. z o.o.
- Vetoquinol S.A.
Responsible authority:
- Ministry Of Health
Authorisation number:
- 102854
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0107/002
Concerned member states:
-
Austria
-
Denmark
-
Germany
-
Greece
-
Italy
-
Portugal
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 3/06/2022
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