Receptal raztopina za injiciranje
Receptal raztopina za injiciranje
Authorised
- Buserelin acetate
Product identification
Medicine name:
Receptal raztopina za injiciranje
Active substance:
- Buserelin acetate
Target species:
-
Cattle (cow)
-
Horse (mare)
-
Pig (female)
-
Rabbit (adult female)
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Buserelin acetate0.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle (cow)
-
Meat and offal, milk0dayMeso in organi: nič dni. Mleko: nič dni
-
- Horse (mare)
-
Meat and offal, milk0dayMeso in organi: nič dni. Mleko: nič dni
-
- Pig (female)
-
Meat and offal0dayMeso in organi: nič dni.
-
- Rabbit (adult female)
-
Meat and offal0dayMeso in organi: nič dni.
-
-
Intravenous use
- Cattle (cow)
-
Meat and offal, milk0dayMeso in organi: nič dni. Mleko: nič dni
-
- Horse (mare)
-
Meat and offal, milk0dayMeso in organi: nič dni. Mleko: nič dni
-
- Pig (female)
-
Meat and offal0dayMeso in organi: nič dni.
-
- Rabbit (adult female)
-
Meat and offal0dayMeso in organi: nič dni.
-
-
Subcutaneous use
- Cattle (cow)
-
Meat and offal, milk0dayMeso in organi: nič dni. Mleko: nič dni
-
- Horse (mare)
-
Meat and offal, milk0dayMeso in organi: nič dni. Mleko: nič dni
-
- Pig (female)
-
Meat and offal0dayMeso in organi: nič dni.
-
- Rabbit (adult female)
-
Meat and offal0dayMeso in organi: nič dni.
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH01CA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovenia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet Deutschland GmbH
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- NP/V/0292/001
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
This document does not exist in this language (English). You can find it
in another language below.
Slovenian (PDF)
Published on: 31/05/2024
Labelling
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in another language below.
Slovenian (PDF)
Published on: 31/05/2024
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Slovenian (PDF)
Published on: 31/05/2024
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