MYXOREN, süstesuspensiooni lüofilisaat ja lahusti küülikutele
MYXOREN, süstesuspensiooni lüofilisaat ja lahusti küülikutele
Authorised
- Myxoma virus, Live
Product identification
Medicine name:
MYXOREN, süstesuspensiooni lüofilisaat ja lahusti küülikutele
Active substance:
- Myxoma virus, Live
Target species:
-
Rabbit (non food-producing)
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Myxoma virus, Live2000.00tissue culture infective dose 501.00dose
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Rabbit (non food-producing)
-
-
Intramuscular use
-
Rabbit (non food-producing)
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI08AD02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Estonia
Package description:
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
- Available only in Estonian
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:
- Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- State Agency Of Medicines
Authorisation number:
- 1481
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.
Estonian (PDF)
Published on: 16/02/2022
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