FOLLIGON, soluzione estemporanea iniettabile per bovini, equini, ovini, caprini, suini, cani, gatti e conigli
FOLLIGON, soluzione estemporanea iniettabile per bovini, equini, ovini, caprini, suini, cani, gatti e conigli
Authorised
- Gonadotropin, equine, serum
- Gonadotropin, equine, serum
Product identification
Medicine name:
FOLLIGON, soluzione estemporanea iniettabile per bovini, equini, ovini, caprini, suini, cani, gatti e conigli
Active substance:
- Gonadotropin, equine, serum
- Gonadotropin, equine, serum
Target species:
-
Dog
-
Cat
-
Cattle
-
Horse
-
Goat
-
Sheep
-
Pig
-
Rabbit
-
Cattle
-
Horse
-
Sheep
-
Goat
-
Pig
-
Cat
-
Dog
-
Rabbit
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Gonadotropin, equine, serum1000.00/international unit(s)1.00Bottle
-
Gonadotropin, equine, serum1000.00/international unit(s)1.00Bottle
Pharmaceutical form:
-
Lyophilisate and solvent for solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Milk0day
-
Meat and offal0day
-
-
Horse
-
Meat and offal0day
-
-
Goat
-
Milk0day
-
Meat and offal0day
-
-
Sheep
-
Milk0day
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
Rabbit
-
Meat and offal0day
-
-
-
Subcutaneous use
-
Cattle
-
Milk0day
-
Meat and offal0day
-
-
Horse
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Goat
-
Meat and offal0day
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
Rabbit
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG03GA03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Available in:
-
Italy
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
- Intervet International GmbH
Responsible authority:
- Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet