CLAVUNOR LC intramammary suspension for lactating cows
CLAVUNOR LC intramammary suspension for lactating cows
Authorised
- Amoxicillin
- Clavulanic acid
- Prednisolone
Product identification
Medicine name:
КЛАВУНОР LC интрамамарна суспензия за лактиращи крави
CLAVUNOR LC intramammary suspension for lactating cows
Active substance:
- Amoxicillin
- Clavulanic acid
- Prednisolone
Target species:
-
Cattle (lactating cow)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Amoxicillin200.00/milligram(s)1.00Syringe
-
Clavulanic acid50.00/milligram(s)1.00Syringe
-
Prednisolone10.00/milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
- Cattle (lactating cow)
-
Meat and offal7dayКрави, чиито месо и вътрешни органи са предназначени за човешка консумация, не подлежат на клане по време на третирането. Крави, чиито месо и вътрешни органи са предназначени за човешка консумация, могат да бъдат заклани 7 дни след последното третиране
-
Milk60hourМляко, предназначено за човешка консумация, не трябва да се използва по време на третирането. Мляко, предназначено за човешка консумация, може да се използва от третираните крави, доени два пъти дневно, 60 часа (т.е. на петото доене) след последното третиране
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51CR02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
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:
- Asklep-Pharma OOD
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories Limited
Responsible authority:
- Bulgarian Agency For Food Safety
Authorisation number:
- 0022-1558
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 7/06/2022
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 7/06/2022
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