Skip to main content
Veterinary Medicines

Rabadrop, Oral suspension

Authorised
  • Rabies virus, strain SAD, Live

Auðkenning lyfsins

Heiti lyfs:
Rabadrop, Oral suspension
RABADROP, oralinė suspensija
Virkt efni:
Íkomuleið:
  • Til inntöku

Upplýsingar um lyfið

Virkt efni / Styrkur:
  • Aðeins í boði í English
    8.50
    log10 tissue culture infective dose 50
    /
    1.00
    Dose
Lyfjaform:
  • Mixtúra, dreifa
Withdrawal period by route of administration:
  • Oral use
    • Fox
    • Raccoon dog
ATC flokkun (dýralyf):
  • QI07BD
Staða markaðsleyfis:
  • Gilt
Authorised in:
  • Litáen
Áletrun:

Viðbótarupplýsingar

Entitlement type:
  • Markaðsleyfi
Markaðsleyfishafi:
  • Bioveta a.s.
Marketing authorisation date:
Framleiðandi sem ber ábyrgð á lokasamþykkt:
  • Bioveta a.s.
Ábyrgt yfirvald:
  • State Food And Veterinary Service
Markaðsleyfisnúmer:
  • LT/2/19/2555/001-005
Dagsetning leyfisbreytingar:
Umsjónarland (RMS):
  • Tékkland
Númer verkferlis:
  • CZ/V/0149/001
Þátttökulönd (CMS):
  • Búlgaría
  • Króatía
  • Eistland
  • Finnland
  • Þýskaland
  • Grikkland
  • Ungverjaland
  • Lettland
  • Litáen
  • Pólland
  • Rúmenía
  • Slóvakía
  • Slóvenía

Skjöl

RV2555.pdf

Lithuanian (PDF)
Birt á: 26/05/2022
Download
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."