Marfloxin 100 mg/ml solution for injection for cattle and pigs
Marfloxin 100 mg/ml solution for injection for cattle and pigs
Authorised
- Marbofloxacin
Product identification
Medicine name:
Marfloxin 100 mg/ml solution for injection for cattle and pigs
Marfloxin 100 mg/ml raztopina za injiciranje za govedo in prašiče
Active substance:
- Marbofloxacin
Target species:
-
Cattle
-
Pig
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous 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:
-
Intramuscular use
-
Cattle
-
Meat and offal4day
-
Meat and offal3dayWhen administered once at 8 mg/kg
-
Milk72hourWhen administered once at 8 mg/kg
-
Milk24hour
-
-
Pig
-
Meat and offal2day
-
-
-
Intravenous use
-
Cattle
-
Meat and offal4day
-
Milk24hour
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal4day
-
Milk24hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA93
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovenia
Available in:
-
Slovenia
Package description:
- 250 ml amber glass vial (Ph. Eur. type II) sealed with a bromobutyl rubber stopper and aluminium closure packaged in an outer carton.
- 100 ml amber glass vial (Ph. Eur. type II) sealed with a bromobutyl rubber stopper and aluminium closure packaged in an outer carton.
- 50 ml amber glass vial (Ph. Eur. type II) sealed with a bromobutyl rubber stopper and aluminium closure packaged in an outer carton.
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:
- KRKA tovarna zdravil d.d. Novo mesto
Marketing authorisation date:
Manufacturing sites for batch release:
- KRKA tovarna zdravil d.d. Novo mesto
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- DC/V/0426/002
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0262/002
Concerned member states:
-
Bulgaria
-
Poland
-
Romania
-
Slovenia
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
