Vectra 3D
-
EU/2/13/156/001
Ceva Sante Animale, Francija
QP53AC54
very 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/2/13/156/001
1
Pipete, 1 deva
-
Vectra 3D
-
EU/2/13/156/017
Ceva Sante Animale, Francija
QP53AC54
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/2/13/156/017
3
Pipete, 1 deva
-
Zulvac BTV
-
EU/2/17/207/003
Zoetis Belgium S.A., Beļģija
QI04AA02
cattle; sheep
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for injection
International name (active substance):
Inactivated bluetongue virus, serotype 1, strain BTV-1/ALG2006/01 E1
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Zoetis Manufacturing Research Spain S L, Spānija
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/2/17/207/003
1
Polietilēna pudele, 120 deva
-
Canigen L4
-
EU/2/15/183/003
Intervet International B.V., Nīderlande
QI07AB01
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for injection
International name (active substance):
L. interrogans serogroup Canicola serovar Portland-vere (strain Ca-12-000),L. interrogans serogroup Icterohaemorrhagiae serovar Copenhageni (strain Ic-02-001),L. interrogans serogroup Australis serovar Bratislava (strain As-05-073),L. kirschneri serogroup Grippotyphosa serovar Dadas (strain Gr-01-005)
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Intervet International B.V., Nīderlande
Date of authorisation/renewal:
02-Jul-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/2/15/183/003
1
Stikla flakons, 10 deva
-
Chanhold
240 mg
EU/2/19/236/013
Chanelle Pharmaceuticals Manufacturing Ltd., Īrija
QP54AA05
dogs 20,1–40,0 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
Chanelle Pharmaceuticals Manufacturing Ltd., Īrija
Date of authorisation/renewal:
17-Apr-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/2/19/236/013
120 mg/ml
3
Plastmasas pipete, 2 ml
-
Zactran
150 mg/ml
EU/2/08/082/004
Boehringer Ingelheim Vetmedica GmbH, Vācija
QJ01FA95
cattle; pigs; sheep
Vairāk
Medicinal product information
Pharmaceutical form:
solution for injection
International name (active substance):
Gamithromycin
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
MERIAL, Francija
Date of authorisation/renewal:
28-Jul-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/2/08/082/004
150 mg/ml
1
Polipropilēna pudelīte, 100 ml
-
Onsior
6 mg
EU/2/08/089/001
Elanco GmbH, Vācija
QM01AH91
cats
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/2/08/089/001
6 mg/tabl.
6
Alumīnija blisteris, 1 tablete
-
Daxocox
15 mg
EU/2/21/270/003
Ecuphar NV, Beļģija
QM01AH95
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
tablets
International name (active substance):
Enflicoxib
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Lelypharma B.V., Nīderlande
Date of authorisation/renewal:
20-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/2/21/270/003
15 mg
3
Blisteris, 4 tablete
-
APOQUEL
5.4 mg/tabl.
EU/2/13/154/013
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/2/13/154/013
5,4 mg/tabl.
1
ABPE pudelīte, 20 tablete
-
Contacera
20 mg/ml
EU/2/12/144/003
Zoetis Belgium S.A., Beļģija
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
Eurovet Animal Health B.V., Nīderlande;Chanelle Pharmaceuticals Manufacturing Ltd., Īrija
Date of authorisation/renewal:
15-Nov-2017
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/2/12/144/003
20 mg/ml
1
Flakons, 100 ml
-
Versican Plus Pi/L4R
-
EU/2/14/173/001
Zoetis Belgium S.A., Beļģija
QI07AJ
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
lyophilisate and solvent for suspension for injection
International name (active substance):
Canine Parainfluenza Type 2 virus, strain CPiV2-Bio15,Inactivated rabies virus, strain SAD Vnukovo-32,Inactivated Leptospira interrogans serovar Canicola, strain MSLB 1090,Leptospira kirschneri serovar Grippotyphosa, strain MSLB 1091,Leptospira interrogans serovar Bratislava, strain MSLB 1088,Leptospira interrogans serovar Icterohaemorrhagia, strain MSLB 1089
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Bioveta, a.s., Čehija
Date of authorisation/renewal:
04-Aug-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/2/14/173/001
25
Stikla flakons, 1 deva
-
Clevor
30 mg/ml
EU/2/17/222/004
Orion Corporation, Somija
QN04BC04
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
eye drops, solution
International name (active substance):
Ropinirole hydrochloride
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Orion Corporation, Somija
Date of authorisation/renewal:
09-Mar-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/2/17/222/004
30 mg/ml
5
ZBPE flakons, 0,6 ml
-
Prevomax
-
EU/2/17/211/002
Dechra Regulatory B.V., Nīderlande
QA04AD90
dogs; cats
Vairāk
Medicinal product information
Pharmaceutical form:
solution for injection
International name (active substance):
Maropitant
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Eurovet Animal Health B.V., Nīderlande;Produlab Pharma b.v., Nīderlande
Date of authorisation/renewal:
11-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/2/17/211/002
1
Stikla flakons, 20 ml
-
Lenivia
0.5 mg
EU/2/25/355/003
Zoetis Belgium S.A., Beļģija
QN02BG93
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
solution for injection
International name (active substance):
Izenivetmab, Izenivetmab
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
21-Nov-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/2/25/355/003
6
I tipa stikla flakons, 1 ml
-
CircoMax
-
EU/2/21/281/005
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/2/21/281/005
10
ABPE flakons, 100 ml
-
Simparica Trio
mg
EU/2/19/243/009
Zoetis Belgium S.A., Beļģija
QP54AB52
Dogs > 5-10 kg
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Sarolaner, Moxidectin, Pyrantel embonate
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Corden Pharma GmbH, Vācija
Date of authorisation/renewal:
17-Sep-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/2/19/243/009
6
Alumīnija folija blisteris, 1 tablete
-
Stronghold Plus
-
EU/2/16/204/006
Zoetis Belgium S.A., Beļģija
QP54AA55
cats
Vairāk
Medicinal product information
Pharmaceutical form:
spot-on solution
International name (active substance):
Selamectin,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:
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/2/16/204/006
6
Polipropilēna pipete, 1 ml
-
Inflacam
5 mg/ml
EU/2/11/134/015
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:
09-Nov-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/2/11/134/015
15 mg/ml
1
Flakons, 10 ml
-
MELOXIDYL
1.5 mg/ml
EU/2/06/070/001
Ceva Sante Animale., Francija
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
Ceva Sante Animale, Francija;Vetem SpA, Itālija
Date of authorisation/renewal:
15-Jan-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/2/06/070/001
1,5 mg/ml
1
Flakons, 10 ml
-
Veraflox
60 mg
EU/2/10/107/007
Bayer Animal Health , Vācija
QJ01MA97
dogs
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/2/10/107/007
60 mg
10
Blisteris, 7 tablete
-