Numelvi
31.6 mg
EU/2/25/351/007
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/2/25/351/007
31,6 mg/tabl.
1
Blisteris, 30 tablete
-
BRAVECTO TriUNO
-
EU/2/24/325/007
Intervet International B.V., Nīderlande
QP54AB52
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
Chewable tablet
International name (active substance):
Fluralaner, Moxidectin, Pyrantel
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
22-Nov-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/2/24/325/007
1
Blisteris, 1 tablete
-
CircoMax Myco
-
EU/2/20/264/001
Zoetis Belgium S.A., Beļģija
QI09AL08
fattening pigs
Vairāk
Medicinal product information
Pharmaceutical form:
emulsion for injection
International name (active substance):
Inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2a ORF2 protein, Inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2b ORF2 protein, Inactivated Mycoplasma hyopneumoniae, strain P-5722-3
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Zoetis Belgium S.A., Beļģija
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/2/20/264/001
1
ABPE flakons, 50 ml
-
Semintra
4 mg/ml
EU/2/12/146/001
Boehringer Ingelheim Vetmedica GmbH, Vācija
QC09CA07
cats
Vairāk
Medicinal product information
Pharmaceutical form:
solution for oral use
International name (active substance):
Telmisartan
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Boehringer Ingelheim Pharma GmbH & Co. KG, Vācija
Date of authorisation/renewal:
28-Feb-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/2/12/146/001
4 mg/ml
1
Flakons, 30 ml
-
LETIFEND
-
EU/2/16/195/005
Laboratorios LETI, S.L. unipersonal, Spānija
QI07A
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
lyophilisate and solvent for solution for injection
International name (active substance):
Recombinant Protein Q from Leishmania infantum MON-1
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
20-Apr-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/2/16/195/005
20
Stikla flakons, 1 deva
-
Porcilis Porcoli Diluvac Forte
-
EU/2/96/001/008
Intervet International Booxmer, Nīderlande
QI09AB02
pigs
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for injection
International name (active substance):
F4ab (K88ab) fimbrial adhesin,F5 (K99) fimbrial adhesin,LT toxoid,F4ac (K88ac) fimbrial adhesin,F6 (987P) fimbrial adhesin
Distribution category:
To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release
Intervet International Booxmer, Nīderlande
Date of authorisation/renewal:
10-Apr-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/2/96/001/008
1
Flakons, 100 ml
-
Syvazul BTV
-
EU/2/18/231/003
Laboratorios SYVA S.A.U, Spānija
QI04AA02
cattle; sheep
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for injection
International name (active substance):
Inactivated bluetongue virus, serotype 4, strain SPA-1/2004
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
LABORATORIOS SYVA, S.A.U. , Spānija
Date of authorisation/renewal:
09-Jan-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/2/18/231/003
1
Polipropilēna flakons, 80 ml
-
APOQUEL
16 mg
EU/2/13/154/036
Zoetis Belgium S.A., Beļģija
QD11AH90
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
Chewable tablet
International name (active substance):
Oclacitinib
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Zoetis Belgium S.A., Beļģija
Date of authorisation/renewal:
04-Jul-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/2/13/154/036
16 mg
5
Blisteris, 10 tablete
-
Metacam
20 mg/ml
EU/2/97/004/027
Boehringer Ingelheim Vetmedica GmbH, Vācija
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
Labiana Life Sciences S.A., Spānija
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/2/97/004/027
20 mg/ml
1
Stikla flakons, 20 ml
-
Advocate Spot-on maziem kaķiem un seskiem
-
EU/2/03/039/019
Bayer Animal Health , Vācija
QP54AB52
ferrets; 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/2/03/039/019
21
Pipete, 0,4 ml
-
Equip WNV
-
EU/2/08/086/004
Zoetis Belgium S.A., Beļģija
QI05AA10
horses
Vairāk
Medicinal product information
Pharmaceutical form:
emulsion for injection
International name (active substance):
Inactivated West Nile V, strain VM-2
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-Sep-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/2/08/086/004
2
Stikla pilnšļirce ar 1 adatu, 1 ml
-
Startvac
-
EU/2/08/092/002
Laboratorios Hipra S.A., Spānija
QI02AB
cattle
Vairāk
Medicinal product information
Pharmaceutical form:
emulsion for injection
International name (active substance):
Inactivated Staphylococcus aureus,Inactivated Escherichia coli
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Laboratorios Hipra S.A., Spānija
Date of authorisation/renewal:
13-Feb-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/2/08/092/002
10
Stikla pudelīte, 1 deva
-
Imoxat
80 mg
EU/2/21/280/008
Chanelle Pharmaceuticals Manufacturing Limited, Īrija
QP54AB52
ferrets; cats
Vairāk
Medicinal product information
Pharmaceutical form:
spot-on solution
International name (active substance):
Imidacloprid, Moxidectin
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Chanelle Pharmaceuticals Manufacturing Ltd., Īrija
Date of authorisation/renewal:
27-Jan-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/2/21/280/008
1
Pipete, 0,8 ml
-
Proteq West Nile
-
EU/2/11/129/002
Boehringer Ingelheim Vetmedica GmbH, Vācija
QI05AX
horses
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for injection
International name (active substance):
Live recombinant canarypox virus
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
MERIAL Laboratoire Porte des Alpes, Francija
Date of authorisation/renewal:
17-May-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/2/11/129/002
1 devas/flakonā
2
Flakons, 1 deva
-
Fluralaner Intervet
400 mg
EU/2/25/346/013
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/2/25/346/013
1
Blisteris, 1 tablete
-
Porcilis PCV M Hyo ID
-
EU/2/24/319/006
Intervet International B.V., Nīderlande
QI09AL08
pigs
Vairāk
Medicinal product information
Pharmaceutical form:
emulsion for injection
International name (active substance):
Porcine circovirus type 2, ORF2 capsid protein
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
30-Aug-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/2/24/319/006
10
PET flakons, 100 deva
-
Equilis Te
-
EU/2/05/055/002
Intervet International Booxmer, Nīderlande
QI05AB03
horses
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for injection
International name (active substance):
Tetanus toxoid
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Intervet International Booxmer, Nīderlande
Date of authorisation/renewal:
12-Jul-2015
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/2/05/055/002
10
Pilnšļirce, 1 deva
-
Onsior
5 mg
EU/2/08/089/007
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/2/08/089/007
5 mg/tabl.
70
Alumīnija blisteris, 1 tablete
-
CircoMax
-
EU/2/21/281/004
Zoetis Belgium S.A., Beļģija
QI09AA07
pigs
Vairāk
Medicinal product information
Pharmaceutical form:
emulsion for injection
International name (active substance):
Inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2a ORF2 protein, Inactivated recombinant chimeric porcine circovirus type 1 containing the porcine circovirus type 2b ORF2 protein
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Zoetis Belgium S.A., Beļģija
Date of authorisation/renewal:
11-Jan-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/2/21/281/004
10
ABPE flakons, 50 ml
-
Vectra 3D
-
EU/2/13/156/031
Ceva Sante Animale, Francija
QP53AC54
medium 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/2/13/156/031
24
Polipropilēna aplikators, 1 deva
-