Marbosol 100 mg/ml solution for injection for cattle and pigs
Marbosol 100 mg/ml solution for injection for cattle and pigs
Authorised
- Marbofloxacin
Product identification
Medicine name:
Marbosol 100 mg/ml solution for injection for cattle and pigs
Marbosol 100 mg/ml Injektionslösung für Rinder und Schweine
Active substance:
- Marbofloxacin
Target species:
-
Cattle
-
Pig
Route of administration:
-
Intravenous use
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Marbofloxacin100.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Cattle
-
Meat and offal6dayMultiple dose (2 mg/kg single daily injection, for 3 to 5 days) (IV/SC/IM)
-
Milk36hourMultiple dose (2 mg/kg single daily injection, for 3 to 5 days) (IV/SC/IM)
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal6dayMultiple dose (2 mg/kg single daily injection, for 3 to 5 days) (IV/SC/IM)
-
Milk36hourMultiple dose (2 mg/kg single daily injection, for 3 to 5 days) (IV/SC/IM)
-
-
-
Intramuscular use
-
Cattle
-
Meat and offal6dayMultiple dose (2 mg/kg single daily injection, for 3 to 5 days) (IV/SC/IM)
-
Milk72hourSingle dose (8 mg/kg) (IM)
-
Milk36hourMultiple dose (2 mg/kg single daily injection, for 3 to 5 days) (IV/SC/IM)
-
Meat and offal3daySingle dose (8 mg/kg) (IM)
-
-
Pig
-
Meat and offal4day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA93
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Available in:
-
Germany
Package description:
- (ID2) 100 millilitre(s): unspecified outer container with 1 Vial (Glass) with 100 millilitre(s)
- (ID1) 50 millilitre(s): unspecified outer container with 1 Vial (Glass) with 50 millilitre(s)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- CP-Pharma Handelsgesellschaft mbH
Marketing authorisation date:
Manufacturing sites for batch release:
- CP-Pharma Handelsgesellschaft mbH
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 401633.00.00
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0175/002
Concerned member states:
-
Hungary
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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