Powerflox 50 mg/ml solution for injection for cattle, pigs, dogs and cats
Powerflox 50 mg/ml solution for injection for cattle, pigs, dogs and cats
Authorised
- Enrofloxacin
Product identification
Medicine name:
Powerflox 50 mg/ml solution for injection for cattle, pigs, dogs and cats
Powerflox 50 mg/ml Injektionslösung für Rinder, Schweine, Hunde und Katzen
Active substance:
- Enrofloxacin
Target species:
-
Cattle (pre-ruminant)
-
Dog
-
Cat
-
Pig
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Enrofloxacin50.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle (pre-ruminant)
-
Meat and offal12day
-
Milkno withdrawal periodNot authorised for use in animals producing milk for human consumption.
-
-
-
Intramuscular use
-
Pig
-
Meat and offal13day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Package description:
- (ID2) 100 millilitre(s): unspecified outer container with 1 Bottle (Glass) with 100 millilitre(s)
- (ID1) 50 millilitre(s): unspecified outer container with 1 Bottle (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:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Virbac
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 401124.00.00
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0183/001
Concerned member states:
-
Austria
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
