Bovaclox DC Xtra intramamálna suspenzia
Bovaclox DC Xtra intramamálna suspenzia
Authorised
- Ampicillin trihydrate
- Cloxacillin hemibenzathine
Product identification
Medicine name:
Bovaclox DC Xtra intramamálna suspenzia
Active substance:
- Ampicillin trihydrate
- Cloxacillin hemibenzathine
Target species:
-
Cattle (dry cow)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Ampicillin trihydrate346.00/milligram(s)1.00Syringe
-
Cloxacillin hemibenzathine1531.00/milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (dry cow)
-
Meat and offal28day
-
Milk156hourDo not administer less than 49 days before calving. If the cow calves less than 49 days after the last treatment, the milk may be used for consumption not earlier than 49 days plus 156 hours after the last treatment. Milk from cows suffering from hypocalcemia can only be used if the maximum residue level is less than 0.03 μg / ml for cloxacillin and 0.004 μg / ml for ampicillin.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51RC26
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories (Ireland) Limited
- Norbrook Laboratories Limited
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/122/99-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Slovak (PDF)
Published on: 23/02/2026
