Taneven 300 mg/ml suspension for injection for horses, cattle, sheep, goats, dogs and cats
Taneven 300 mg/ml suspension for injection for horses, cattle, sheep, goats, dogs and cats
Authorised
- Benzylpenicillin procaine monohydrate
Product identification
Medicine name:
Taneven 300 mg/ml suspension for injection for horses, cattle, sheep, goats, dogs and cats
Taneven
Active substance:
- Benzylpenicillin procaine monohydrate
Target species:
-
Cattle
-
Dog
-
Goat
-
Sheep
-
Horse
-
Cat
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Benzylpenicillin procaine monohydrate300.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Meat and offal10day
-
Milk120hour
-
- Dog
- Goat
-
Milk120hour
-
Meat and offal10day
-
- Sheep
-
Meat and offal10day
-
Milk120hour
-
- Horse
-
Meat and offal10day
-
Milkno withdrawal periodNot authorised for use mares producing milk for human consumption.
-
- Cat
-
Intramuscular use
- Cattle
-
Meat and offal10day
-
Milk120hour
-
- Dog
- Goat
-
Milk120hour
-
Meat and offal10day
-
- Sheep
-
Meat and offal10day
-
Milk120hour
-
- Horse
-
Meat and offal10day
-
Milkno withdrawal periodNot authorised for use mares producing milk for human consumption.
-
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CE09
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Available in:
-
Germany
Package description:
- (ID1) 100 millilitre(s): Box (Cardboard) with 1 Vial (Glass) with 100 millilitre(s), closed with Cap and Stopper (Aluminium, bromobutyl rubber`)
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:
- Wirtschaftsgenossenschaft deutscher Tieraerzte eG
Marketing authorisation date:
Manufacturing sites for batch release:
- Wirtschaftsgenossenschaft Deutscher Tieraerzte eG
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 402721.00.00
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0337/001
Concerned member states:
-
Austria
-
Bulgaria
-
Hungary
-
Italy
-
Luxembourg
-
Poland
-
Romania
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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