Veyxyl Tabs 800 mg/tbl. na perorálnu aplikáciu pre psy 800 mg/tbl. na intrauterinnú aplikáciu pre kravy, ovce, prasnice a kobyly
Veyxyl Tabs 800 mg/tbl. na perorálnu aplikáciu pre psy 800 mg/tbl. na intrauterinnú aplikáciu pre kravy, ovce, prasnice a kobyly
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Veyxyl Tabs 800 mg/tbl. na perorálnu aplikáciu pre psy 800 mg/tbl. na intrauterinnú aplikáciu pre kravy, ovce, prasnice a kobyly
Active substance:
- Amoxicillin trihydrate
Target species:
-
Dog
-
Cattle (cow)
-
Pig (sow)
-
Sheep (ewe)
-
Horse (mare)
Route of administration:
-
Oral use
-
Intrauterine use
Product details
Active substance and strength:
-
Amoxicillin trihydrate918.40milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Withdrawal period by route of administration:
-
Oral use
-
Dog
-
-
Intrauterine use
-
Cattle (cow)
-
Meat and offal4day
-
Milk1day
-
-
Pig (sow)
-
Meat and offal4day
-
-
Sheep (ewe)
-
Meat and offal4day
-
Milk1day
-
-
Horse (mare)
-
Meat and offal4day
-
Milk1day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG51AA03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Package description:
- Available only in Slovak
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Veyx Pharma GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Veyx Pharma GmbH
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/0631/96-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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