GESTAVET HCG 200 / PMSG 400 (40 IU/ml + 80 IU/ml) lyophilisate and solvent for solution for injection for pigs
GESTAVET HCG 200 / PMSG 400 (40 IU/ml + 80 IU/ml) lyophilisate and solvent for solution for injection for pigs
Authorised
- Gonadotropin, equine, serum
- Chorionic gonadotrophin, human
Product identification
Medicine name:
GESTAVET HCG 200 / PMSG 400 (40 IU/ml + 80 IU/ml) lyophilisate and solvent for solution for injection for pigs
Active substance:
- Gonadotropin, equine, serum
- Chorionic gonadotrophin, human
Target species:
-
Pig (sow)
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Gonadotropin, equine, serum400.00/international unit(s)1.00Vial
-
Chorionic gonadotrophin, human200.00/international unit(s)1.00Vial
Pharmaceutical form:
-
Lyophilisate and solvent for solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig (sow)
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG03GA99
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Package description:
- box containing 5 vials of lyophilisate and 5 vials of 5 ml of solvent
- box containing 10 vials of lyophilisate and box containing 10 vials of 5 ml of solvent
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Biogenesis Global S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Hipra S.A.
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 401256.00.00
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0134/001
Concerned member states:
-
Austria
-
Belgium
-
France
-
Germany
-
Greece
-
Italy
-
Lithuania
-
Malta
-
Netherlands
-
Portugal
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet