RAFENDAZOL 10 mg/g + 8 mg/g premix na medikáciu krmiva pre raticovú zver
RAFENDAZOL 10 mg/g + 8 mg/g premix na medikáciu krmiva pre raticovú zver
Authorised
- Rafoxanide
- Mebendazole
Product identification
Medicine name:
RAFENDAZOL 10 mg/g + 8 mg/g premix na medikáciu krmiva pre raticovú zver
Active substance:
- Rafoxanide
- Mebendazole
Target species:
-
Red deer
-
Fallow deer
-
Roe deer
-
Mouflon
-
Chamois
Route of administration:
-
In-feed use
Product details
Active substance and strength:
-
Rafoxanide10.00milligram(s)1.00gram(s)
-
Mebendazole8.00milligram(s)1.00gram(s)
Pharmaceutical form:
-
Premix for medicated feeding stuff
Withdrawal period by route of administration:
-
In-feed use
- Red deer
-
Meat and offal28day
-
- Fallow deer
-
Meat and offal28day
-
- Roe deer
-
Meat and offal28day
-
- Mouflon
-
Meat and offal60day
-
- Chamois
-
Meat and offal60day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP52AC59
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:
- BIOPHARM Vyzkumny ustav biofarmacie a veterinarnich leciv a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
- Biopharm Research Institute Of Biopharmacy And Veterinary Drugs a.s.
Responsible authority:
- USKVBL
Authorisation number:
- 98/184/85-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: 15/11/2021
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