Orbenin Extra Dry Cow 600 mg, intrammamary suspension for cattle
Orbenin Extra Dry Cow 600 mg, intrammamary suspension for cattle
Authorised
- Cloxacillin
Product identification
Medicine name:
Orbenin Extra Dry Cow 600 mg, интрамамарна суспензия за говеда
Orbenin Extra Dry Cow 600 mg, intrammamary suspension for cattle
Active substance:
- Cloxacillin
Target species:
-
Cattle
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Cloxacillin600.00/milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle
-
Meat and offal28day
-
Milk96hourМляко: 96 часа след отелване. Не се препоръчва при крави с по – къс от 42 дни сухостоен период.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CF02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Available 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:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- HAUPT PHARMA LATINA
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-1642
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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in another language below.
Bulgarian (PDF)
Published on: 27/03/2025
Package Leaflet
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in another language below.
Bulgarian (PDF)
Published on: 27/03/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 27/03/2025