Emevet
-
EU/2/25/343/006
CP-Pharma Handelsgesellschaft GmbH, Vācija
QA04AD90
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Maropitant
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
02-Jun-2025
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/25/343/006
3
Blisteris, 10 tablete
-
Vectra 3D
-
EU/2/13/156/009
Ceva Sante Animale, Francija
QP53AC54
small dogs
Vairāk
Medicinal product information
Pharmaceutical form:
spot-on solution
International name (active substance):
Permethrin,Pyriproxyfen,Dinotefuran
Distribution category:
Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release
Ceva Sante Animale, Francija
Date of authorisation/renewal:
27-Aug-2018
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/13/156/009
12
Pipete, 1 deva
-
Vectra 3D
-
EU/2/13/156/025
Ceva Sante Animale, Francija
QP53AC54
very large dogs
Vairāk
Medicinal product information
Pharmaceutical form:
spot-on solution
International name (active substance):
Permethrin,Pyriproxyfen,Dinotefuran
Distribution category:
Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release
Ceva Sante Animale, Francija
Date of authorisation/renewal:
27-Aug-2018
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/13/156/025
48
Pipete, 1 deva
-
Ultifend ND IBD
-
EU/2/21/272/001
Ceva-Phylaxia Veterinary Biologicals Co. Ltd., Ungārija
QI01AD16
chickens; embryonated chicken eggs
Vairāk
Medicinal product information
Pharmaceutical form:
concentrate and solvent for suspension for injection
International name (active substance):
Cell-associated live recombinant turkey herpesvirus (rHVT/ND/IBD), expressing the fusion protein ofNewcastle disease virus and the VP2 protein of infectious bursal disease virus
Distribution category:
To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release
Ceva-Phylaxia Veterinary Biologicals Co. Ltd., Ungārija
Date of authorisation/renewal:
20-Apr-2021
Marketing authorisation valid until:
19-Apr-2026
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/21/272/001
1
Stikla ampula, 1000 deva
-
APOQUEL
3.6 mg
EU/2/13/154/001
Zoetis Belgium S.A., Beļģija
QD11AH90
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
film-coated tablets
International name (active substance):
Oclacitinib
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Pfizer Italia S.R.L., Itālija
Date of authorisation/renewal:
26-Jul-2018
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/13/154/001
1
Blisteris, 20 tablete
-
Credelio
450 mg
EU/2/17/206/012
Elanco GmbH, Vācija
QP53BE04
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Lotilaner
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Elanco France S.A.S, Francija
Date of authorisation/renewal:
26-Apr-2022
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/17/206/012
450 mg
1
Alumīnija blisteris, 6 tablete
-
Veraflox
15 mg
EU/2/10/107/002
Bayer Animal Health , Vācija
QJ01MA97
dogs; cats
Vairāk
Medicinal product information
Pharmaceutical form:
tablets
International name (active substance):
Pradofloxacin
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
KVP Pharma + Veterinar Produkte GmbH, Vācija
Date of authorisation/renewal:
07-Jan-2016
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/10/107/002
15 mg
3
Blisteris, 7 tablete
-
Stronghold
45 mg
EU/2/99/014/008
Zoetis Belgium S.A., Beļģija
QP54AA05
cats
Vairāk
Medicinal product information
Pharmaceutical form:
spot-on solution
International name (active substance):
Selamectin
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Pfizer Service Company bvba, Beļģija
Date of authorisation/renewal:
01-Oct-2009
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/99/014/008
45 mg/deva
6
Polipropilēna pudelīte, 1 deva
-
Tulissin
25 mg/ml
EU/2/20/252/008
VIRBAC, Francija
QJ01FA94
pigs
Vairāk
Medicinal product information
Pharmaceutical form:
solution for injection
International name (active substance):
Tulathromycin
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
FAREVA AMBOISE, Francija;VIRBAC, Francija
Date of authorisation/renewal:
24-Apr-2020
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/20/252/008
25 mg/ml
1
Stikla flakons, 20 ml
-
BRAVECTO CombiUNO
-
EU/2/25/350/008
Intervet International B.V., Nīderlande
QP54AB51
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Fluralaner, Milbemycin oxime
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
30-Jul-2025
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/25/350/008
3
Blisteris, 1 tablete
-
Aivlosin
625 mg/g
EU/2/04/044/019
ECO Animal Health Europe Limited, Īrija
QJ01FA92
chickens; turkeys
Vairāk
Medicinal product information
Pharmaceutical form:
granules for use in drinking water
International name (active substance):
Tylvalosin (as Tylvalosin tartrate)
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Cod Beck Blenders Limited, Lielbritānija
Date of authorisation/renewal:
17-Jun-2009
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/04/044/019
1
Alumīnija folijas maisiņš, 400 g
-
Reconcile
32 mg
EU/2/08/080/003
FORTE Healthcare Limited, Īrija
QN06AB03
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Fluoxetine hydrochloride
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Eli Lilly and Company Limited, Lielbritānija
Date of authorisation/renewal:
13-Jul-2018
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/08/080/003
32 mg/tabl.
30
ABPE pudele, 1 tablete
-
Rabitec
-
EU/2/17/219/001
Ceva Sante Animale,, Francija
QI07BD
raccoon dogs; foxes
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for oral use
International name (active substance):
Attenuated live rabies virus
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
07-Oct-2022
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/17/219/001
1
Polimēra maiss, 800 deva
-
DRAXXIN
100 mg/ml
EU/2/03/041/001
Zoetis Belgium S.A., Beļģija
QJ01FA94
cattle; pigs; sheep
Vairāk
Medicinal product information
Pharmaceutical form:
solution for injection
International name (active substance):
Tulathromycin
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
FAREVA AMBOISE, Francija;Zoetis Belgium S.A., Beļģija
Date of authorisation/renewal:
19-Aug-2008
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/03/041/001
100 mg/ml
1
Stikla flakons, 20 ml
-
Masivet
50 mg
EU/2/08/087/001
AB Science S.A., Francija
QL01XE90
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
film-coated tablets
International name (active substance):
Masitinib
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
CRID PHARMA, Francija;Centre Spécialités Pharmaceutiques, Francija
Date of authorisation/renewal:
17-Nov-2008
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/08/087/001
50 mg/tabl.
30
Pudelīte, 1 tablete
-
Fluralaner Intervet
560 mg
EU/2/25/346/020
Intervet International B.V., Nīderlande
QP53BE02
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Fluralaner
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
27-Jun-2025
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/25/346/020
6
Blisteris, 1 tablete
-
Emepax 160 mg
160 mg
EU/2/26/363/011
Axience, Francija
QA04AD90
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Maropitant citrate monohydrate
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Lelypharma B.V., Nīderlande
Date of authorisation/renewal:
26-Mar-2026
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/26/363/011
1
OPA/Al/PVH-Al blisteris, 4 tablete
-
EVICTO
45 mg
EU/2/19/242/005
VIRBAC, Francija
QP54AA05
cats 2,6 - 7,5 kg
Vairāk
Medicinal product information
Pharmaceutical form:
spot-on solution
International name (active substance):
Selamectin
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
VIRBAC, Francija
Date of authorisation/renewal:
19-Jul-2019
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/19/242/005
60 mg/ml
4
Polipropilēna pipete, 0,75 ml
-
Equilis Prequenza
-
EU/2/05/056/001
Intervet International B.V., Nīderlande
QI05AA01
horses
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for injection
International name (active substance):
A/equine-2/Newmarket/1/93,A/equine-2/Newmarket/2/93,Purified haemagglutinin subunits from equine influenza viruses: A/equine-1/Praque/1/56
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Intervet International Booxmer, Nīderlande
Date of authorisation/renewal:
08-Jul-2005
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/05/056/001
10
Stikla flakons, 1 deva
[PDF]
Eluracat
20 mg/ml
EU/2/23/297/002
Elanco GmbH, Vācija
QH01AX90
cats
Vairāk
Medicinal product information
Pharmaceutical form:
solution for oral use
International name (active substance):
Capromorelin
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
29-Jun-2023
Marketing authorisation valid until:
Unlimited time period
Marketing authorisation procedure:
EU
Package leaflet:
*
-
Labelling text:
*
-
Summary of product characteristics:
*
-
*
More detailed information available on the European Medicines Agency website
Products
ID
Strength
Package size
Primary packaging
Labelling
EU/2/23/297/002
1
Flakons, 15 ml
-