Folligon 200 IU/ml lyofilizát na injekčný roztok
Folligon 200 IU/ml lyofilizát na injekčný roztok
Not authorised
- Serum gonadotrophin
- Serum gonadotrophin
Product identification
Medicine name:
Folligon 200 IU/ml lyofilizát na injekčný roztok
Active substance:
- Serum gonadotrophin
- Serum gonadotrophin
Target species:
-
Cattle (cow)
-
Cattle (heifer)
-
Sheep (ewe)
-
Goat (adult female)
-
Pig (sow)
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Serum gonadotrophin5000.00/international unit(s)1.00Vial
-
Serum gonadotrophin1000.00/international unit(s)1.00Vial
Pharmaceutical form:
-
Lyophilisate and solvent for solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle (cow)
-
Meat and offal0dayZero days.
-
-
Cattle (heifer)
-
Meat and offal0dayZero days.
-
-
Sheep (ewe)
-
Meat and offal0dayZero days.
-
-
Goat (adult female)
-
Meat and offal0dayZero days.
-
-
Pig (sow)
-
Meat and offal0dayZero days.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG03GA03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Slovakia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (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.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/044/10-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 26/01/2022