MASTICEN SECADO, intramaminė suspensija
MASTICEN SECADO, intramaminė suspensija
Autoriseret
- Cloxacillin hemibenzathine
Produktidentifikation
Lægemiddelnavn:
MASTICEN SECADO, intramaminė suspensija
Aktiv substans:
- Kun tilgængelig på English
Dyreart:
-
Ko
-
Får
-
Ged
Administrationsvej:
-
Intramammær anvendelse
Produktoplysninger
Aktiv substans og styrke:
-
Kun tilgængelig på English1000.00/milligram(s)1.00Sprøjte
Lægemiddelform:
-
Intramammær suspension
Tilbageholdelsestid efter administrationsrute:
-
Intramammær anvendelse
-
Ko
-
Meat and offal0dagIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
Milk0dagIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
-
Får
-
Meat and offal0dagIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
Milk0dagIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
-
Ged
-
Meat and offal0dagIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
Milk0dagIf the drug was administered 28 days before giving birth. If the drying period is less than 4 weeks, milk has to be tested for antibiotics residue.
-
-
Anatomisk terapeutisk kemisk veterinær (ATCvet) kode:
- QJ51CF02
Godkendelsesstatus:
-
Gyldig
Pakningsbeskrivelse:
- Kun tilgængelig på Lithuanian
- Kun tilgængelig på Lithuanian
Yderligere oplysninger
Indehaver af markedsføringstilladelsen:
- Vetmarket UAB
Dato for markedsføringstilladelse:
Fremstillere ansvarlige for batchfrigivelse:
- Cenavisa S.L.
Ansvarlig myndighed:
- State Food And Veterinary Service
Markedsføringstilladelsesnummer:
- LT/2/02/1410/001-002
Dato for ændring af godkendelsesstatus:
Indberetninger om formodede bivirkninger på veterinærlægemidler: www.adrreports.eu/vet
Dokumenter
Combined File of all Documents
Dette dokument findes ikke på dette sprog (dansk). Du kan finde det på et andet sprog nedenfor.
Lithuanian (PDF)
Udgivet den: 23/12/2025
