Emevet
-
EU/2/25/343/008
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/2/25/343/008
10
Blisteris, 10 tablete
-
Trilorale
50 mg/ml
EU/2/24/313/006
Axience, Francija
QH02CA01
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
Oral solution
International name (active substance):
Trilostane
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
06-May-2024
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/2/24/313/006
50 mg/ml
1
Polipropilēna pudele, 50 ml
-
Broadline
-
EU/2/13/157/006
Boehringer Ingelheim Vetmedica GmbH, Vācija
QP54AA54
large cats
Vairāk
Medicinal product information
Pharmaceutical form:
spot-on solution
International name (active substance):
Fipronil,Praziquantel,S-Methoprene,Eprinomectin
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Merial, Francija
Date of authorisation/renewal:
24-Sep-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/2/13/157/006
4
Polipropilēna aplikators, 1 deva
-
Advocate Spot-on lieliem kaķiem
-
EU/2/03/039/021
Bayer Animal Health , Vācija
QP54AB52
cats
Vairāk
Medicinal product information
Pharmaceutical form:
spot-on solution
International name (active substance):
Moxidectin,Imidacloprid
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:
01-Apr-2003
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/2/03/039/021
21
Pipete, 0,8 ml
-
NEXGARD SPECTRA
-
EU/2/14/177/013
Boehringer Ingelheim Vetmedica GmbH, Vācija
QP54AB51
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Milbemycin oxime,Afoxolaner
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Merial, Francija
Date of authorisation/renewal:
15-Feb-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/2/14/177/013
1
PVH/Aclar/Al blisteris, 1 tablete
-
Lotimax
225 mg
EU/2/24/311/003
Elanco GmbH, Vācija
QP53BE04
dogs 5,1–10,0 kg
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
-
Date of authorisation/renewal:
25-Apr-2024
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/2/24/311/003
225 mg
1
Alumīnija blisteris, 3 tablete
-
Loxicom
50 mg/g
EU/2/08/090/030
Norbrook Laboratories (Ireland) Limited, Īrija
QM01AC06
horses
Vairāk
Medicinal product information
Pharmaceutical form:
paste for oral use
International name (active substance):
Meloxicam
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Norbrook Laboratories Limited, Lielbritānija
Date of authorisation/renewal:
12-Mar-2014
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/2/08/090/030
50 mg/g
7
Šļirce, 8,4 g
-
Suiseng Diff/A
-
EU/2/21/278/004
Laboratorios Hipra S.A., Spānija
QI09AB12
pigs
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for injection
International name (active substance):
Clostridioides difficile, toxoid A (TcdA), Clostridioides difficile, toxoid B (TcdB), Clostridium perfringens type A, α-toxoid
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Laboratorios Hipra S.A., Spānija
Date of authorisation/renewal:
07-Dec-2021
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/2/21/278/004
1
PET flakons, 100 ml/25 deva
-
ZULVAC 1+8 Ovis
-
EU/2/11/120/003
Zoetis Belgium S.A., Beļģija
QI02AA08
sheep
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for injection
International name (active substance):
Bluetongue virus serotype 8 antigen,Bluetongue virus serotype 1 antigen
Distribution category:
To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release
Zoetis Manufacturing & Research Spain S.L., Spānija
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/2/11/120/003
1
Flakons, 120 deva
-
Melosus
1.5 mg/ml
EU/2/10/116/005
CP-Pharma Handelsgesellschaft GmbH, Vācija
QM01AC06
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for oral use
International name (active substance):
Meloxicam
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Produlab Pharma b.v., Nīderlande
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/2/10/116/005
1,5 mg/ml
1
Pudele, 10 ml
-
DRAXXIN
100 mg/ml
EU/2/03/041/005
Zoetis Belgium S.A., Beļģija
QJ01FA94
cattle
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/2/03/041/005
100 mg/ml
1
Stikla pudelīte, 500 ml
-
Sileo
0.1 mg/ml
EU/2/15/181/003
Orion Corporation, Somija
QN05CM18
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
oromucosal gel
International name (active substance):
Dexmedetomidine hydrochloride
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Orion Corporation, Somija
Date of authorisation/renewal:
09-Jun-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/2/15/181/003
0,1 mg/ml
5
polietilēna šļirce, 3 ml
-
Lotilaner Elanco
12 mg
EU/2/22/288/011
Elanco GmbH, Vācija
QP53BE04
cats
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:
13-Sep-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/2/22/288/011
12 mg
1
Blisteris, 1 tablete
-
Loxicom
1 mg
EU/2/08/090/022
Norbrook Laboratories (Ireland) Limited, Īrija
QM01AC06
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Meloxicam
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Norbrook Laboratories Limited, Lielbritānija
Date of authorisation/renewal:
12-Mar-2014
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/2/08/090/022
1 mg
50
Blisteris, 10 tablete
-
Vectormune HVT-AIV
-
EU/2/25/335/003
Ceva Sante Animale,, Francija
QI01AD
chickens
Vairāk
Medicinal product information
Pharmaceutical form:
concentrate and solvent for suspension for injection
International name (active substance):
Turkey herpesvirus, strain rHVT/AI-H5 (FC126, cell-associated), expressing haemagglutinin gene of Avian influenza virus subtype H5, Live
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
28-Mar-2025
Marketing authorisation valid until:
27-Mar-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/2/25/335/003
1
Stikla ampula, 4000 deva
-
Neptra
-
EU/2/19/246/003
Bayer Animal Health , Vācija
QS02CA91
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
ear drops, solution
International name (active substance):
Florfenicol, Terbinafine hydrochloride, Mometasone fuorate
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
KVP Pharma und Veterinär - Produkte GmbH, Vācija
Date of authorisation/renewal:
10-Dec-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/2/19/246/003
20
Tūbiņa, 1 ml
-
Porcilis AR - T DF
-
EU/2/00/026/001
Intervet International Booxmer, Nīderlande
QI09AB04
pigs
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for injection
International name (active substance):
Inactivated Bordetella bronchiseptica, Pasteurella multocida toxoid
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Intervet International Booxmer, Nīderlande
Date of authorisation/renewal:
08-Feb-2006
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/2/00/026/001
1
Flakons, 10 deva
-
Porcilis PCV M Hyo
-
EU/2/14/175/007
Intervet International B.V., Nīderlande
QI09AL
fattening pigs
Vairāk
Medicinal product information
Pharmaceutical form:
emulsion for injection
International name (active substance):
Inactivated Mycoplasma hyopneumoniae,Inactivated recombinant Porcine Circovirus type 2
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Intervet International B.V., Nīderlande
Date of authorisation/renewal:
30-Nov-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/2/14/175/007
10
PET pudele, 25 deva
-
Innovax-ND-IBD-ILT
-
EU/2/25/347/002
Intervet International B.V., Nīderlande
-
chickens; embryonated chicken eggs
Vairāk
Medicinal product information
Pharmaceutical form:
concentrate and solvent for suspension for injection
International name (active substance):
Turkey herpesvirus, strain HVT/ND/IBD/ILT, expressing fusion protein gene of NDV and VP2 protein gene of IBD virus and gD and gI glycoproteins genes of ILT virus, Live
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
04-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/2/25/347/002
1
Stikla ampula, 4000 deva
-
Credelio
450 mg
EU/2/17/206/010
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/2/17/206/010
450 mg
1
Alumīnija blisteris, 1 tablete
-