Receptal 4.2 µg/ml Oplossing voor injectie
Receptal 4.2 µg/ml Oplossing voor injectie
Authorised
- Buserelin acetate
Product identification
Medicine name:
Receptal 4.2 µg/ml Oplossing voor injectie
Receptal 4.2 µg/ml Solution injectable
Receptal 4.2 µg/ml Injektionslösung
Active substance:
- Buserelin acetate
Target species:
-
Rabbit
-
Cattle
-
Horse
-
Pig
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Buserelin acetate4.20microgram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Rabbit
-
Meat and offalno withdrawal period0 days
-
- Cattle
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
- Horse
-
Meat and offalno withdrawal period0 days
-
- Pig
-
Meat and offalno withdrawal period0 days
-
-
Intravenous use
- Pig
-
Meat and offalno withdrawal period0 days
-
- Rabbit
-
Meat and offalno withdrawal period0 days
-
- Horse
-
Meat and offalno withdrawal period0 days
-
- Cattle
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
-
Subcutaneous use
- Horse
-
Meat and offalno withdrawal period0 days
-
- Pig
-
Meat and offalno withdrawal period0 days
-
- Rabbit
-
Meat and offalno withdrawal period0 days
-
- Cattle
-
Meat and offalno withdrawal period0 days
-
Meat and offalno withdrawal period0 days
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH01CA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Receptal 5 50 ml Vial Solution for injection
- Receptal 50 ml Vial Solution for injection
- Receptal 5 10 ml Vial Solution for injection
- Receptal 5 5 ml Vial Solution for injection
- Receptal 5 2.5 ml Vial Solution for injection
- Receptal 10 ml Vial Solution for injection
- Receptal 5 ml Vial Solution for injection
- Receptal 2.5 ml Vial Solution for injection
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 GmbH
Responsible authority:
- FAMHP
Authorisation number:
- BE-V118781
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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Package Leaflet
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