Valemas 50 mg/ml Solution for Injection for Cattle, Sheep, Goats, Pigs, Dogs and Cats
Valemas 50 mg/ml Solution for Injection for Cattle, Sheep, Goats, Pigs, Dogs and Cats
Authorised
- Enrofloxacin
Product identification
Medicine name:
VALEMAS 50 mg/ml solution for injection for cattle, sheep, goats, pigs, dogs and cats.
Valemas 50 mg/ml Solution for Injection for Cattle, Sheep, Goats, Pigs, Dogs and Cats
Active substance:
- Enrofloxacin
Target species:
-
Pig
-
Cattle
-
Dog
-
Goat
-
Sheep
-
Cat
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Enrofloxacin50.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
Meat and offal13day
-
-
-
Intravenous use
-
Cattle
-
Meat and offal5day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal12day
-
-
Dog
-
Goat
-
Meat and offal6day
-
Milk96hour
-
-
Sheep
-
Meat and offal4day
-
Milk72hour
-
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
United Kingdom (Northern Ireland)
Available in:
-
United Kingdom (Northern Ireland)
Package description:
- The product is presented in amber Type II glass bottle of 50 ml with chlorobutyl rubber stopper sealed with a flip-off aluminium cap with a tamper-evident polypropylene seal.
- The product is presented in amber Type II glass bottle of 100 ml with chlorobutyl rubber stoppers sealed with a flip-off aluminium cap with a tamper-evident polypropylene seal.
- The product is presented in amber Type II glass bottle of 250 ml with chlorobutyl rubber stoppers sealed with a flip-off aluminium cap with a tamper-evident polypropylene seal.
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:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A
Responsible authority:
- The Veterinary Medicines Directorate
Authorisation number:
- Vm 11557/4003
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0445/001
Concerned member states:
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 3/05/2024
How useful was this page?: