Uniferon 200 mg/ml solution for injection
Uniferon 200 mg/ml solution for injection
Authorised
This information is not available for this product.
Product identification
Medicine name:
Uniferon 200 mg/ml solution for injection
UNIFERON 200 MG/ML SOLUTION INJECTABLE
Active substance:
This information is not available for this product.
Target species:
-
Pig
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
This information is not available for this product.
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Pig
-
Intramuscular use
- Pig
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QB03AC
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Package description:
- 20 x 100 ml vials (glass) in a carton box
- 12 x 100 ml vials (LDPE) in a carton box
- 5 x 100 ml vials (LDPE) in a carton box
- 5 x 100 ml vials (HDPE) in a carton box
- 12 x 100 ml vials (HDPE) in a carton box
- 20 x 100 ml vials (LDPE) in a carton box
- 5 x 100 ml vials (glass) in a carton box
- 20 x 100 ml vials (HDPE) in a carton box
- 12 x 100 ml vials (glass) in a carton box
- 12 x 200 ml vials in a carton box
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Pharmacosmos A/S
Marketing authorisation date:
Manufacturing sites for batch release:
- Pharmacosmos A/S
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/4085166 8/2010
Date of authorisation status change:
Reference member state:
-
Denmark
Procedure number:
- DK/V/0114/001
Concerned member states:
-
Czechia
-
Estonia
-
Finland
-
France
-
Germany
-
Iceland
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 16/10/2023
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 17/11/2023
PI.pdf
English (PDF)
Download Published on: 27/01/2022
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