Ampiclox Quick Release 75 mg/3 g - 200 mg/3 g Suspensie voor intramammair gebruik
Ampiclox Quick Release 75 mg/3 g - 200 mg/3 g Suspensie voor intramammair gebruik
Authorised
- Cloxacillin sodium
- Ampicillin sodium
Product identification
Medicine name:
Ampiclox Quick Release 75 mg/3 g - 200 mg/3 g Suspensie voor intramammair gebruik
Ampiclox Quick Release 75 mg/3 g - 200 mg/3 g Suspension intramammaire
Ampiclox Quick Release 75 mg/3 g - 200 mg/3 g Suspension zur intramammären Anwendung
Active substance:
- Cloxacillin sodium
- Ampicillin sodium
Target species:
-
Cattle
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Cloxacillin sodium218.40milligram(s)3.00gram(s)
-
Ampicillin sodium79.70milligram(s)3.00gram(s)
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
- Cattle
-
Meat and offal2day
-
Milk60hour
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51CF02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Ampiclox Quick Release 30 3 g Tube Intramammary suspension
- Ampiclox Quick Release 24 3 g Tube Intramammary suspension
- Ampiclox Quick Release 12 3 g Tube Intramammary suspension
- Ampiclox Quick Release 3 3 g Tube Intramammary suspension
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Haupt Pharma Latina S.r.l.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V095645
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
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Package Leaflet
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