Benestermycin suspensija ievadīšanai tesmenī liellopiem
Benestermycin suspensija ievadīšanai tesmenī liellopiem
Authorised
- Benethamine penicillin
- Framycetin sulfate
- Penethamate hydriodide
Product identification
Medicine name:
Benestermycin suspensija ievadīšanai tesmenī liellopiem
Active substance:
- Benethamine penicillin
- Framycetin sulfate
- Penethamate hydriodide
Target species:
-
Cattle (dry cow)
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Benethamine penicillin280.00milligram(s)1.00Syringe
-
Framycetin sulfate100.00milligram(s)1.00Syringe
-
Penethamate hydriodide100.00milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
-
Cattle (dry cow)
-
Meat and offal8dayPienam: - ja ārstēšana notikusi vismaz 35 dienas pirms dzemdībām, pienu nedrīkst lietot 36 stundas pēc dzemdībām; - ja ārstēšana notikusi mazāk nekā 35 dienas pirms dzemdībām, pienu nedrīkst lietot 37 dienas pēc ārstēšanas.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51RC25
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
Package description:
- Available only in Latvian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Boehringer Ingelheim Vetmedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Haupt Pharma Latina S.r.l.
- Lohmann Pharma Herstellung GmbH
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/NRP/96/0294
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 3/06/2024
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