Rabisin
- Inaktivēts trakumsērgas vīruss, celms G52
-
Valid
Authorised in these countries:
-
Germany
Product identification
Medicine name:
Rabisin
Active substance and strength:
-
Inaktivēts trakumsērgas vīruss, celms G52
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AA02
Authorisation number:
- 94a/84
Product identification number:
- ac6e12cf-9999-4df6-bed2-f2fab6e1c1cd
Permanent identification number:
- 600000073327
Product details
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Sheep
-
Meat and offal0day
-
Milk0day
-
- Dog
- Mustelids
- Cattle
-
Milk0day
-
Meat and offal0day
-
- Cat
- Horse
-
Milk0day
-
Meat and offal0day
-
-
Subcutaneous use
- Cattle
-
Milk0day
-
Meat and offal0day
-
- Sheep
-
Meat and offal0day
-
Milk0day
-
- Dog
- Mustelids
- Horse
-
Milk0day
-
Meat and offal0day
-
- Cat
Availability
Package description:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.
Authorisation details
Authorisation status:
-
Valid
Authorisation procedure type:
-
Marketing Authorisation
Procedure number:
- 2603390
Date of authorisation status change:
Legal basis of product authorisation:
-
Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Authorisation country:
-
Germany
Responsible authority:
- PEI
Marketing authorisation holder:
- Boehringer Ingelheim Vetmedica GmbH
Marketing authorisation issued:
Reference member state:
This information is not available for this product.
Concerned member states:
This information is not available for this product.
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.
Additional information
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
First published:
Last updated:
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