Geepenil® vet.24 g, powder and solvent for solution for injection
Geepenil® vet.24 g, powder and solvent for solution for injection
Authorised
- Benzylpenicillin sodium
Product identification
Medicine name:
Geepenil® vet.24 g, powder and solvent for solution for injection
Geepenil vet 24 g stungulyfsstofn og leysir, laus
Active substance:
- Benzylpenicillin sodium
Target species:
-
Cattle
-
Pig
-
Horse
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Benzylpenicillin sodium24.00/gram(s)1.00Vial
Pharmaceutical form:
-
Powder and solvent for solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal10day
-
Milk2day
-
-
Pig
-
Meat and offal10day
-
-
-
Intravenous use
-
Horse
-
Meat and offal10day
-
-
Cattle
-
Meat and offal10day
-
Milk2day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CE01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Iceland
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Orion Corporation
Marketing authorisation date:
Manufacturing sites for batch release:
- Orion Oyj / Orion Corporation / Orion Pharma
Responsible authority:
- Icelandic Medicines Agency
Authorisation number:
- IS/2/12/004/01
Date of authorisation status change:
Reference member state:
-
Sweden
Procedure number:
- SE/V/0118/001
Concerned member states:
-
Iceland
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: 28/07/2025
Icelandic (PDF)
Published on: 13/09/2024
Updated on: 15/12/2025
Package Leaflet
English (PDF)
Download Published on: 28/07/2025
Icelandic (PDF)
Published on: 13/09/2024
Updated on: 15/12/2025