Simparica
80 mg/tabl.
EU/2/15/191/014
Zoetis Belgium S.A., Beļģija
QP53BE03
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Sarolaner
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Zoetis Belgium S.A., Beļģija
Date of authorisation/renewal:
12-Aug-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/2/15/191/014
1
Al/Al blisteris, 3 tablete
-
ArthriCox
57 mg
EU/2/24/323/001
Chanelle Pharmaceuticals Manufacturing Limited, Īrija
QM01AH90
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Firocoxib
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
24-Oct-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/2/24/323/001
30
Alumīnija folija blisteris, 1 tablete
-
CEVAC REOMUNE
-
EU/2/25/334/001
Filavie, Francija
QI01AA04
chickens
Vairāk
Medicinal product information
Pharmaceutical form:
emulsion for injection
International name (active substance):
Avian reovirus, strain S1133, Inactivated
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
28-Aug-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/2/25/334/001
1
Polipropilēna pudele, 500 ml
-
NexGard
28.3 mg/tabl.
EU/2/13/159/006
Boehringer Ingelheim Vetmedica GmbH, Vācija
QP53BE01
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Afoxolaner
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
MERIAL, Francija
Date of authorisation/renewal:
13-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/2/13/159/006
28,3 mg/tabl.
1
PVH/Aclar/Al blisteris, 6 tablete
-
DIVENCE TETRA
2 ml
EU/2/24/310/003
Laboratorios Hipra S.A., Spānija
QI02AH
cattle
Vairāk
Medicinal product information
Pharmaceutical form:
lyophilisate and solvent for emulsion for injection
International name (active substance):
Bovine viral diarrhoea virus 1, E2 protein, recombinant, Bovine viral diarrhoea virus 2, E2 protein, recombinant, Bovine herpesvirus 1, strain CEDDEL, gE- tk- double-gene deleted, Live, Bovine parainfluenza virus 3, strain SF-4, Inactivated, Bovine respiratory syncytial virus, strain Lym-56, Live
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
10-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/2/24/310/003
2 ml
1
Stikla flakons, 20 devas/flakonā
-
Credelio Plus
-
EU/2/21/271/011
Elanco GmbH, Vācija
QP54AB51
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Lotilaner, Milbemycin oxime
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:
14-Apr-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/2/21/271/011
1
Al/Al blisteris, 6 tablete
-
Onsior
5 mg
EU/2/08/089/006
Elanco GmbH, Vācija
QM01AH91
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
tablets
International name (active substance):
Robenacoxib
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Elanco France S.A.S, Francija;Vericore Ltd., Lielbritānija
Date of authorisation/renewal:
15-Dec-2013
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/2/08/089/006
5 mg/tabl.
28
Alumīnija blisteris, 1 tablete
-
Rheumocam
5.0 mg/ml
EU/2/07/078/015
Chanelle Pharmaceuticals Manufacturing Ltd., Īrija
QM01AC06
dogs; cats
Vairāk
Medicinal product information
Pharmaceutical form:
solution for injection
International name (active substance):
Meloxicam
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Chanelle Pharmaceuticals Manufacturing Ltd., Īrija
Date of authorisation/renewal:
18-Dec-2012
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/2/07/078/015
5 mg/ml
1
Stikla flakons, 10 ml
-
Enteroporc Coli AC
-
EU/2/20/262/005
Ceva Sante Animale,, Francija
QI09AB08
gilt; Pregnant sow
Vairāk
Medicinal product information
Pharmaceutical form:
lyophilisate and suspension for suspension for injection
International name (active substance):
Clostridium perfringens alpha toxoid, Clostridium perfringens beta1 toxoid, Clostridium perfringens beta2 toxoid, F4ab fimbrial adhesin of E. coli, F4ac fimbrial adhesin of E. coli, F5 fimbrial adhesin of E. coli, F6 fimbrial adhesin of E. coli
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
IDT Biologika GmbH, Vācija
Date of authorisation/renewal:
09-Dec-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/2/20/262/005
1
Flakons (suspensija ZBPE pudelē), 25 deva
-
Equioxx
57 mg
EU/2/08/083/008
AUDEVARD , Francija
QM01AH90
horses
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Firocoxib
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Merial, Francija
Date of authorisation/renewal:
06-Jun-2013
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/2/08/083/008
57 mg
18
PVH/Al blisteris (caurspīdīgs), 10 tablete
-
Recocam
20 mg/ml
EU/2/11/133/001
Bimeda Animal Health Limited, Īrija
QM01AC06
cattle; pigs; horses
Vairāk
Medicinal product information
Pharmaceutical form:
solution for injection
International name (active substance):
Meloxicam
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Accord Healthcare Limited, Lielbritānija
Date of authorisation/renewal:
09-Aug-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/2/11/133/001
20 mg/ml
1
Stikla flakons, 10 ml
-
Profender tablets for small dogs
-
EU/2/05/054/022
Vetoquinol S.A., Francija
QP52AA51
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
modified-release tablets
International name (active substance):
Praziquantel,Emodepside
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:
29-Jul-2010
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/2/05/054/022
15 mg/3 mg
50
Alumīnija blisteris, 1 tablete
-
Mastijet Forte
-
V/I/21/0068
Intervet International BV, Nīderlande
QJ51RV01
lactating cows
Vairāk
Medicinal product information
Pharmaceutical form:
intramammary suspension
International name (active substance):
Tetracycline, Neomycin, Bacitracin, Prednisolone
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Intervet International Booxmer, Nīderlande
Date of authorisation/renewal:
09-Nov-2021
Marketing authorisation valid until:
08-Nov-2026
Marketing authorisation procedure:
I
Package leaflet:
[DOCX] Mastijet_Forte_PL_2023_06 (06-Jul-2023)
Labelling text:
See products section
Summary of product characteristics:
-
Products
ID
Strength
Package size
Primary packaging
Labelling
V/I/21/0068-01
20
Polipropilēna šļirce, 8 g
[PDF]
Senvelgo
15 mg/ml
EU/2/23/305/002
Boehringer Ingelheim Vetmedica GmbH, Vācija
QA10BK90
cats
Vairāk
Medicinal product information
Pharmaceutical form:
Oral solution
International name (active substance):
Velagliflozin
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
20-Nov-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/2/23/305/002
15 mg/ml
1
ABPE pudele, 12 ml
[DOCX]
[DOCX]
[DOCX]
Credelio Plus
-
EU/2/21/271/014
Elanco GmbH, Vācija
QP54AB51
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Lotilaner, Milbemycin oxime
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:
14-Apr-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/2/21/271/014
1
Al/Al blisteris, 3 tablete
-
Metacam
1 mg
EU/2/97/004/044
Boehringer Ingelheim Vetmedica GmbH, Vācija
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
Boehringer Ingelheim Vetmedica GmbH, Vācija
Date of authorisation/renewal:
06-Dec-2007
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/2/97/004/044
1 mg
84
Blisteris, 1 tablete
-
Numelvi
7.2 mg
EU/2/25/351/004
Intervet International B.V., Nīderlande
QD11AH93
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
tablets
International name (active substance):
Atinvicitinib
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
24-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/2/25/351/004
7,2 mg/tabl.
3
Blisteris, 30 tablete
-
Drontal Plus Flavour
-
V/I/21/0045
Bayer Animal Health GmbH, Vācija
QP52AA51
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
tablets
International name (active substance):
Febantel, Pyrantel, Praziquantel
Distribution category:
Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release
KVP Pharma und Veterinär - Produkte GmbH, Vācija
Date of authorisation/renewal:
09-Aug-2021
Marketing authorisation valid until:
08-Aug-2026
Marketing authorisation procedure:
I
Package leaflet:
[DOCX] 082021LI (09-Aug-2021)
Labelling text:
See products section
Summary of product characteristics:
-
Products
ID
Strength
Package size
Primary packaging
Labelling
V/I/21/0045-01
2
PP/PP blisteris, 1 tablete
-
HEPIZOVAC
-
EU/2/25/341/002
CZ Vaccines S.A.U., Spānija
QI02AA
cattle
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for injection
International name (active substance):
Epizootic haemorrhagic disease virus, serotype 8, strain EHDV8 SPA 2022/LCV_03 LCV Cod.:O78, Inactivated
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
23-Apr-2025
Marketing authorisation valid until:
22-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/2/25/341/002
1
ABPE pudele, 100 ml
-
NASYM
-
EU/2/19/241/004
Laboratorios Hipra S.A., Spānija
QI02AD04
cattle
Vairāk
Medicinal product information
Pharmaceutical form:
Lyophilisate and solvent for suspension for injection or nasal spray
International name (active substance):
Live attenuated bovine respiratory syncytial virus, strain Lym-56
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Laboratorios Hipra S.A., Spānija
Date of authorisation/renewal:
29-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/2/19/241/004
10
Stikla flakons, 25 devas/flakonā
-