Suigonan Vet. pulver og solvens til injektionsvæske, opløsning 2000 IE + 1000 IE
Suigonan Vet. pulver og solvens til injektionsvæske, opløsning 2000 IE + 1000 IE
Authorised
- Serum gonadotrophin
- Chorionic gonadotrophin
- Serum gonadotrophin
- Chorionic gonadotrophin
Product identification
Medicine name:
Suigonan Vet. pulver og solvens til injektionsvæske, opløsning 2000 IE + 1000 IE
Active substance:
- Serum gonadotrophin
- Chorionic gonadotrophin
- Serum gonadotrophin
- Chorionic gonadotrophin
Target species:
-
Pig
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Serum gonadotrophin2000.00/international unit(s)1.00Dose
-
Chorionic gonadotrophin1000.00/international unit(s)1.00Dose
-
Serum gonadotrophin2000.00/international unit(s)1.00Dose
-
Chorionic gonadotrophin1000.00/international unit(s)1.00Dose
Pharmaceutical form:
-
Powder and solvent for solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Pig
-
Meat and offal6dayKassation af injektionssted ved slagtning inden 6 døgn efter behandling.
-
Meat and offal6dayKassation af injektionssted ved slagtning inden 6 døgn efter behandling.
-
Meat and offal6dayKassation af injektionssted ved slagtning inden 6 døgn efter behandling.
-
Meat and offal6dayKassation af injektionssted ved slagtning inden 6 døgn efter behandling.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG03GA99
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Denmark
Available in:
-
Denmark
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International GmbH
- Intervet International B.V.
Responsible authority:
- Danish Medicines Agency
Authorisation number:
- 10430
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Danish (, PULVER OG SOLVENS TIL INJEKTIONSVÆSKE, OPLØSNING)
Published on: 16/09/2024