NexGard Spectra 37.5 mg + 7.5 mg - Chewable tablet

Įgaliotas

Afoxolaner
Milbemycin oxime

Download as PDF

Vaisto identifikaciniai duomenys

Vaisto pavadinimas:

NexGard Spectra 37.5 mg + 7.5 mg - Chewable tablet

Veiklioji medžiaga:

Pateikiama tik English
Pateikiama tik English

Paskirties gyvūnų rūšis (-ys):

Šuo

Naudojimo būdas:

Vartoti per burną

Vaisto duomenys

Veiklioji medžiaga / Stiprumas:

Pateikiama tik English

Presentation_strength:37.5 mg Reference:In house Index:0
Pateikiama tik English

Presentation_strength:7.5 mg Reference:In house Index:1

Vaisto forma:

Kramtomoji tabletė

Withdrawal period by route of administration:

Vartoti per burną
- Šuo

Anatominės, terapinės ir cheminės veterinarinių vaistų klasifikacijos (ATCvet) kodas:

QP54AB51

Tiekimo teisinis statusas:

Pateikiama tik Czech Estonian English French Italian Latvian Portuguese Slovenian Finnish Swedish Icelandic Norwegian

Registracijos statusas:

Valid

Authorised in:

Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Croatian Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian Greek English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Latvian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish German Estonian English French Italian Dutch Portuguese Slovak Finnish Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Romanian Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Croatian Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Spanish Czech German Estonian English French Italian Dutch Portuguese Slovak Swedish Icelandic Norwegian
Pateikiama tik Estonian English French Swedish Icelandic Norwegian

Pakuotės aprašymas:

Pateikiama tik English
Pateikiama tik English
Pateikiama tik English
Pateikiama tik English
Pateikiama tik English

Papildoma informacija

Entitlement type:

Pateikiama tik English French Croatian Italian Latvian Finnish Swedish Icelandic Norwegian

Vaisto registracijos teisinis pagrindas:

Pateikiama tik English Italian Latvian Norwegian

Registruotojas:

Boehringer Ingelheim Vetmedica GmbH

Marketing authorisation date:

15/01/2015

Serijos išleidimo gamybos vietos:

Boehringer Ingelheim Animal Health France

Atsakinga institucija:

European Commission

Registracijos pažymėjimo numeris:

Šios informacijos apie šį preparatą nėra.

Registracijos statuso pasikeitimo data:

15/01/2015

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Dokumentai

Combined File of all Documents

lietuvių (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Kitos kalbos (24)

Bulgarian (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Croatian (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Czech (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Danish (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Dutch (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

English (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Estonian (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Finnish (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

French (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

German (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Greek (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Hungarian (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Icelandic (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Italian (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Latvian (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Maltese (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Norwegian (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Polish (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Portuguese (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Romanian (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Slovak (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Slovenian (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Spanish (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

Swedish (PDF)

Paskelbta: 15/03/2024

Parsisiųsti

ema-puar-v3842-nexgard-spectra-ws2280-g-vra-0034-g-en.pdf

English (PDF)

Paskelbta: 25/09/2023

Parsisiųsti

ema-puar-nexgard-spectra-nex-spe-var-ws1338-en.pdf

English (PDF)

Paskelbta: 15/03/2023

Parsisiųsti

ema-puar-nexgard-spectra-v-3842-par-en.pdf

English (PDF)

Paskelbta: 15/03/2023

Parsisiųsti

ema-puar-nexgard-spectra-v-3842-var-ii-0008-en.pdf

English (PDF)

Paskelbta: 15/03/2023

Parsisiųsti

ema-puar-nexgard-spectra-v-3842-var-ii-0019-en.pdf

English (PDF)

Paskelbta: 15/03/2023

Parsisiųsti

ema-puar-nexgard-spectra-nex-spe-var-ws1559-en.pdf

English (PDF)

Paskelbta: 15/03/2023

Parsisiųsti

Įvertinkite, kiek naudingas šis puslapis:

NexGard Spectra 37.5 mg + 7.5 mg - Chewable tablet

Vaisto identifikaciniai duomenys

Vaisto duomenys

Papildoma informacija

Dokumentai

Produkto informacija

Viešojo vertinimo ataskaita (-os)