FERROFERON 200 mg/ml Solution for injection for pigs
FERROFERON 200 mg/ml Solution for injection for pigs
Authorised
- Gleptoferron
Product identification
Medicine name:
FERROFERON 200 mg/ml Solution for injection for pigs
Ferroferon 200 mg/ml
Active substance:
- Gleptoferron
Target species:
-
Pig (sucking piglet)
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Gleptoferron532.60milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Pig (sucking piglet)
-
Meat and offal0day
-
-
Intramuscular use
- Pig (sucking piglet)
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QB03AC
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Package description:
- (ID6) 2000 millilitre(s): unspecified outer container with 10 Vial (Low Density PolyEthylene) each with 200 millilitre(s)
- (ID5) 200 millilitre(s): unspecified outer container with 1 Vial (Low Density PolyEthylene) with 200 millilitre(s)
- (ID4) 1000 millilitre(s): unspecified outer container with 10 Vial (Low Density PolyEthylene) each with 100 millilitre(s)
- (ID3) 100 millilitre(s): unspecified outer container with 1 Vial (Low Density PolyEthylene) with 100 millilitre(s)
- (ID2) 1000 millilitre(s): unspecified outer container with 10 Vial (Glass) each with 100 millilitre(s)
- (ID1) 100 millilitre(s): unspecified outer container with 1 Vial (Glass) with 100 millilitre(s)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Informed consent application (Article 13c of Directive No 2001/82/EC)
Marketing authorisation holder:
- Iron4u ApS
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva Sante Animale
- Serumwerk Bernburg AG
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 401405.00.00
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0157/001
Concerned member states:
-
Belgium
-
Denmark
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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