Quiflor 100 mg/ml solution for injection for cattle and pigs (sows)
Quiflor 100 mg/ml solution for injection for cattle and pigs (sows)
Authorised
- Marbofloxacin
Product identification
Medicine name:
Quiflor 100 mg/ml solution for injection for cattle and pigs (sows)
Quiflor 100 mg/ml injekcinis tirpalas galvijams ir kiaulėms (paršavedėms)
Active substance:
- Marbofloxacin
Target species:
-
Cattle
-
Pig (sow for reproduction)
Route of administration:
-
Intravenous use
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Marbofloxacin100.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
- Cattle
-
Milk36hour
-
Meat and offal6day
-
-
Subcutaneous use
- Cattle
-
Milk36hour
-
Meat and offal6day
-
-
Intramuscular use
- Cattle
-
Milk36hour
-
Meat and offal6day
-
- Pig (sow for reproduction)
-
Meat and offal4day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA93
Legal status of supply:
This information is not available for this product.
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Package description:
- (ID3) 50 millilitre(s): unspecified outer container with 1 Vial (Glass) with 50 millilitre(s), closed with Stopper (bromobutyl rubber`)
- (ID2) 100 millilitre(s): unspecified outer container with 1 Vial (Glass) with 100 millilitre(s), closed with Stopper (bromobutyl rubber`)
- (ID1) 250 millilitre(s): unspecified outer container with 1 Vial (Glass) with 250 millilitre(s), closed with Stopper (bromobutyl rubber`)
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 d.d. Novo Mesto
- Tad Pharma GmbH
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/11/2042/001-003
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0302/001
Concerned member states:
-
Austria
-
Belgium
-
Denmark
-
Greece
-
Italy
-
Lithuania
-
Netherlands
-
Portugal
-
Slovakia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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