URSOFERRAN 200 mg/ml Solution for injection for pigs
URSOFERRAN 200 mg/ml Solution for injection for pigs
Not authorised
- Gleptoferron
Product identification
Medicine name:
URSOFERRAN 200 mg/ml Solution for injection for pigs
Active substance:
- Gleptoferron
Target species:
-
Pig (suckling piglet)
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Gleptoferron532.60/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig (suckling piglet)
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QB03AC
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Luxembourg
Package description:
- (ID6): 1 unspecified outer container with 10 Vial (Low Density PolyEthylene) with 200 millilitre(s) (2000 millilitre(s))
- (ID5): 1 unspecified outer container with 1 Vial (Low Density PolyEthylene) with 200 millilitre(s) (200 millilitre(s))
- (ID4): 1 unspecified outer container with 10 Vial (Low Density PolyEthylene) with 100 millilitre(s) (1000 millilitre(s))
- (ID3): 1 unspecified outer container with 10 Vial (Glass) with 100 millilitre(s) (1000 millilitre(s))
- (ID2): 1 unspecified outer container with 1 Vial (Low Density PolyEthylene) with 100 millilitre(s) (100 millilitre(s))
- (ID1): 1 unspecified outer container with 1 Vial (Glass) with 100 millilitre(s) (100 millilitre(s))
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Serumwerk Bernburg AG
Marketing authorisation date:
Manufacturing sites for batch release:
- Serumwerk Bernburg AG
- Ceva Sante Animale
Responsible authority:
- Ministere De La Sante Division De La Pharmacie Et Des Medicaments
Authorisation number:
- V 877/13/02/1268
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0149/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
How useful was this page?:
