Taneven LC 3 g intramammary suspension for lactating cows
Taneven LC 3 g intramammary suspension for lactating cows
Authorised
- Benzylpenicillin procaine monohydrate
Product identification
Medicine name:
Taneven LC 3 g intramammary suspension for lactating cows
Taneven LC 3 g suspensão intramamária para bovinos
Active substance:
- Benzylpenicillin procaine monohydrate
Target species:
-
Cattle
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Benzylpenicillin procaine monohydrate3.00gram(s)20.00gram(s)
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
- Cattle
-
Milk120hour
-
Meat and offal5day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51CE09
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Package description:
- (ID4) 1600 gram(s): Box with 80 Syringe (High Density PolyEthylene) each with 20 gram(s), closed with Lid (Low Density PolyEthylene)
- (ID3) 400 gram(s): Box with 20 Syringe (High Density PolyEthylene) each with 20 gram(s), closed with Lid (Low Density PolyEthylene)
- (ID2) 240 gram(s): Box with 12 Syringe (High Density PolyEthylene) each with 20 gram(s), closed with Lid (Low Density PolyEthylene)
- (ID1) 200 gram(s): Box with 10 Syringe (High Density PolyEthylene) each with 20 gram(s), closed with Lid (Low Density PolyEthylene)
- (ID6) 240 gram(s): Box with 12 Syringe (Low Density PolyEthylene) each with 20 gram(s), closed with Lid (Low Density PolyEthylene)
- (ID8) 1600 gram(s): Box with 80 Syringe (Low Density PolyEthylene) each with 20 gram(s), closed with Lid (Low Density PolyEthylene)
- (ID5) 200 gram(s): Box with 10 Syringe (Low Density PolyEthylene) each with 20 gram(s), closed with Lid (Low Density PolyEthylene)
- (ID7) 400 gram(s): Box with 20 Syringe (Low Density PolyEthylene) each with 20 gram(s), closed with Lid (Low Density PolyEthylene)
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:
- Directorate General For Food And Veterinary
Authorisation number:
- 1354/01/20RFVPT
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0338/001
Concerned member states:
-
Austria
-
Bulgaria
-
Hungary
-
Ireland
-
Luxembourg
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Sweden
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 11/02/2022
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