ORBENIN DRY COW, 500mg, Intramamární suspenze
ORBENIN DRY COW, 500mg, Intramamární suspenze
Authorised
- Cloxacillin hemibenzathine
Product identification
Medicine name:
ORBENIN DRY COW, 500mg, Intramamární suspenze
Active substance:
- Cloxacillin hemibenzathine
Target species:
-
Cattle
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Cloxacillin hemibenzathine638.00milligram(s)1.00Applicator
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle
-
Meat and offal28day
-
Milk96hourpo porodu v případě období stání na sucho 35 dní a více. 35 dní plus 96 hodin v případě období stání na sucho kratším než 35 dní. Přípravek nesmí být použit v laktaci, ale výhradně v období stání na sucho.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51CF02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Czechia
Available in:
-
Czechia
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 Ceska Republika s.r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- HAUPT PHARMA LATINA
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/256/91-C
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.
Czech (PDF)
Published on: 12/01/2024
Package Leaflet
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in another language below.
Czech (PDF)
Published on: 12/01/2024
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 12/01/2024
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