VIRBACTAN 150 MG INTRAMAMMARY OINTMENT
VIRBACTAN 150 MG INTRAMAMMARY OINTMENT
Authorised
- Cefquinome sulfate
Product identification
Medicine name:
VIRBACTAN 150 MG INTRAMAMMARY OINTMENT
Virbactan 150 mg pomada intramamária
Active substance:
- Cefquinome sulfate
Target species:
-
Cattle (cow)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Cefquinome sulfate177.80milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary ointment
Withdrawal period by route of administration:
-
Intramammary use
- Cattle (cow)
-
Meat and offal2day
-
Milk36dayMilk: 36 days after treatment when dry period is 5 weeks or less.
-
Milk1dayMilk: 1 day after calving when dry period is more than 5 weeks
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51DE90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Available in:
-
Portugal
Package description:
- Box of 1 sachet of 4 applicators and 4 cleaning towels
- Box of 5 sachets of 4 applicators and 20 cleaning towels
- Box of 6 sachets of 4 applicators and 24 cleaning towels
- Box of 15 sachets of 4 applicators and 60 cleaning towels
- Box of 30 sachets of 4 applicators and 120 cleaning towels
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Haupt Pharma Latina S.r.l.
- Virbac
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- 51551
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0148/001
Concerned member states:
-
Austria
-
Belgium
-
Cyprus
-
Czechia
-
Estonia
-
Germany
-
Greece
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Poland
-
Portugal
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Portuguese (PDF)
Published on: 15/11/2023
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