Cefa Safe 300 mg Intramammary Suspension for dairy cows at drying-off
Cefa Safe 300 mg Intramammary Suspension for dairy cows at drying-off
Authorised
- Cefapirin benzathine
Product identification
Medicine name:
Cefa Safe 300 mg Intramammary Suspension for dairy cows at drying-off
CEFA SAFE 300 MG/10ML ΕΝΔΟΜΑΣΤΙΚΟ ΕΝΑΙΩΡΗΜΑ
Active substance:
- Cefapirin benzathine
Target species:
-
Cattle (dairy cow at drying-off)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Cefapirin benzathine383.30milligram(s)1.00Applicator
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (dairy cow at drying-off)
-
Meat and offal14day
-
Milk24hour24 hours after calving if the interval between treatment and calving is 32 days or longer.
-
Milk33day33 days after treatment if the interval between treatment and calving is less than 32 days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51DB08
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Package description:
- (ID2) 1440 millilitre(s): Behältnis (Plastic) with 144 Syringe (Low Density PolyEthylene) each with 10 millilitre(s), closed with Lid (Low Density PolyEthylene)
- (ID1) 200 millilitre(s): Box (Cardboard) with 20 Syringe (Low Density PolyEthylene) each with 10 millilitre(s), closed with Lid (Low Density PolyEthylene)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 144677/27-12-2022/K-0246701
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0339/001
Concerned member states:
-
Austria
-
Belgium
-
Croatia
-
Cyprus
-
Czechia
-
Estonia
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Portugal
-
Romania
-
Slovakia
-
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
English (PDF)
Download Published on: 23/10/2024
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