Febrivac DIST, süstesuspensiooni lüofilisaat ja lahusti minkidele ja tuhkrutele
Febrivac DIST, süstesuspensiooni lüofilisaat ja lahusti minkidele ja tuhkrutele
Authorised
- Canine distemper virus, strain Lederle D84/1, Live
Product identification
Medicine name:
Febrivac DIST, süstesuspensiooni lüofilisaat ja lahusti minkidele ja tuhkrutele
Active substance:
- Canine distemper virus, strain Lederle D84/1, Live
Target species:
-
Mink
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Canine distemper virus, strain Lederle D84/1, Live5012.00/tissue culture infective dose 501.00dose
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Mink
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI20CD01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Estonia
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:
- IDT Biologika GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- IDT Biologika GmbH
Responsible authority:
- State Agency Of Medicines
Authorisation number:
- 1160
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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Estonian (PDF)
Published on: 14/02/2022
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