CENFLOX 100 mg/ml solution for injection for cattle and pigs
CENFLOX 100 mg/ml solution for injection for cattle and pigs
Authorised
- Enrofloxacin
Product identification
Medicine name:
CENFLOX 100 mg/ml solution for injection for cattle and pigs
Cenflox 100 mg/ml šķīdums injekcijām liellopiem un cūkām
Active substance:
- Enrofloxacin
Target species:
-
Cattle
-
Pig
Route of administration:
-
Subcutaneous use
-
Intravenous use
-
Intramuscular use
Product details
Active substance and strength:
-
Enrofloxacin100.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offalno withdrawal periodMeat and offal: s.c.: 14 days/i.v.: 7 days
-
-
Cattle
-
Milkno withdrawal periodMilk: sc: 120 houras (5 days)/i.v 72 hours (3 days)
-
-
-
Intravenous use
-
Cattle
-
Meat and offalno withdrawal periodMeat and offal: s.c.: 14 days/i.v.: 7 days
-
-
Cattle
-
Milkno withdrawal periodMilk: sc: 120 houras (5 days)/i.v 72 hours (3 days)
-
-
-
Intramuscular use
-
Pig
-
Meat and offal12day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
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:
- Cenavisa S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- Cenavisa S.L.
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/DCP/19/0018
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0296/001
Concerned member states:
-
Bulgaria
-
Croatia
-
Czechia
-
Hungary
-
Latvia
-
Lithuania
-
Portugal
-
Romania
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
