Laurabolin 25 mg/ml solution for injection
Laurabolin 25 mg/ml solution for injection
Authorised
- Nandrolone laurate
Product identification
Medicine name:
Laurabolin 25 mg/ml solution for injection
Active substance:
- Nandrolone laurate
Target species:
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Nandrolone laurate25.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Dog
-
Cat
-
-
Subcutaneous use
-
Dog
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA14AB01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- Hydrolytic Type I glass vial with rubber stopper, closed with a colour coded aluminium cap. Each vial contains 10 ml solution.
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 (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International GmbH
- INTERVET INTERNATIONAL B.V.
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10996/002/001
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
English (PDF)
Download Published on: 3/05/2024
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