Penovet vet. 300 mg/ml injeksjonsvæske, suspensjon
Penovet vet. 300 mg/ml injeksjonsvæske, suspensjon
Authorised
- Benzylpenicillin procaine
Product identification
Medicine name:
Penovet vet. 300 mg/ml injeksjonsvæske, suspensjon
Active substance:
- Benzylpenicillin procaine
Target species:
-
Cattle
-
Pig
-
Sheep
-
Goat
-
Horse
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
-
Subcutaneous use
-
Intrauterine use
-
Intrasynovial use
-
Intraperitoneal use
Product details
Active substance and strength:
-
Benzylpenicillin procaine300.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Milk3day
-
Meat and offal14day
-
-
Pig
-
Meat and offal5day
-
-
Sheep
-
Meat and offal14day
-
Milk3day
-
-
Goat
-
Milk3day
-
Meat and offal14day
-
-
Horse
-
Milk3day
-
Meat and offal14day
-
-
-
Subcutaneous use
-
Horse
-
Milk3day
-
Meat and offal14day
-
-
Cattle
-
Milk3day
-
Meat and offal14day
-
-
Sheep
-
Meat and offal14day
-
Milk3day
-
-
Goat
-
Milk3day
-
Meat and offal14day
-
-
Pig
-
Meat and offal5day
-
-
-
Intrauterine use
-
Cattle
-
Milk3day
-
Meat and offal6day
-
-
Goat
-
Milk3day
-
Meat and offal6day
-
-
Horse
-
Milk3day
-
Meat and offal6day
-
-
Sheep
-
Milk3day
-
Meat and offal6day
-
-
Pig
-
Meat and offal6day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CE09
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Norway
Available in:
-
Norway
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Boehringer Ingelheim Animal Health Denmark A/S
Marketing authorisation date:
Manufacturing sites for batch release:
- KELA Kempisch Laboratorium Kela Laboratoria
Responsible authority:
- Norwegian Medical Products Agency
Authorisation number:
- 00-04323
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Norwegian (PDF)
Published on: 19/03/2025
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Norwegian (PDF)
Published on: 19/03/2025