Coxatab
57 mg
EU/2/22/286/009
CP-Pharma Handelsgesellschaft GmbH, Vācija
QM01AH90
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
Chewable tablet
International name (active substance):
Firocoxib
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
CP-Pharma Handelsgesellschaft GmbH, Vācija
Date of authorisation/renewal:
12-Aug-2022
Marketing authorisation valid until:
11-Aug-2027
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/2/22/286/009
57 mg/tabl.
1
alumīnija/PVC/PE/PVDC blisteris, 30 tablete
-
BRAVECTO TriUNO
-
EU/2/24/325/005
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/2/24/325/005
3
Blisteris, 1 tablete
-
Tulinovet
100 mg/ml
EU/2/20/257/002
V.M.D. n.v., 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
V.M.D. n.v., Beļģija;Laboratoires Biove, Francija
Date of authorisation/renewal:
16-Sep-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/2/20/257/002
1
Stikla flakons un flakons, 50 ml
-
FRONTPRO
28.3 mg
EU/2/19/240/006
Boehringer Ingelheim Vetmedica GmbH, Vācija
QP53BE01
Dogs >4–10 kg
Vairāk
Medicinal product information
Pharmaceutical form:
chewable tablets
International name (active substance):
Afoxolaner
Distribution category:
Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release
Merial, Francija
Date of authorisation/renewal:
20-May-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/2/19/240/006
28,3 mg
1
PVH/Aclar/Al blisteris, 3 tablete
-
Fluralaner Intervet
200 mg
EU/2/25/346/011
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/2/25/346/011
3
Blisteris, 1 tablete
-
Bovilis INtranasal RSP Live
-
V/I/23/0046
Intervet International B.V., Nīderlande
QI02AD07
cattle
Vairāk
Medicinal product information
Pharmaceutical form:
nasal spray, lyophilisate and solvent for suspension
International name (active substance):
Live bovine respiratory syncytial virus, strain Jencine-2013, Live bovine parainfluenza virus type 3, strain INT2-2013
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Intervet International B.V., Nīderlande
Date of authorisation/renewal:
20-Sep-2023
Marketing authorisation valid until:
19-Sep-2028
Marketing authorisation procedure:
I
Package leaflet:
[DOCX] 23052024LI (23-May-2024)
Labelling text:
See products section
Summary of product characteristics:
-
Products
ID
Strength
Package size
Primary packaging
Labelling
V/I/23/0046-01
1
Stikla flakons, 5 deva
[PDF]
[PDF]
V/I/23/0046-02
5
Stikla flakons, 5 deva
[PDF]
[PDF]
[PDF]
GALLIPRANT
100 mg
EU/2/17/221/006
Elanco GmbH, Vācija
QM01AX92
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
tablets
International name (active substance):
Grapiprant
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
09-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/2/17/221/006
100 mg
30
Polietilēna pudele, 30 tablete
-
Oestrophan
0.25 mg/ml
V/I/19/0077
Bioveta, a.s., Čehija
QG02AD90
sows; mares; cows
Vairāk
Medicinal product information
Pharmaceutical form:
solution for injection
International name (active substance):
Cloprostenol
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Bioveta, a.s., Čehija
Date of authorisation/renewal:
16-Dec-2024
Marketing authorisation valid until:
15-Dec-2029
Marketing authorisation procedure:
I
Package leaflet:
[DOCX] 16122024_LI (16-Dec-2024)
Labelling text:
See products section
Summary of product characteristics:
-
Products
ID
Strength
Package size
Primary packaging
Labelling
V/I/19/0077-01
0,25 mg
10
Stikla ampula, 2 ml
[PDF]
[PDF]
V/I/19/0077-02
0,25 mg
1
Stikla flakons, 10 ml
[PDF]
[PDF]
Covexin 10
-
V/I/24/0063
Zoetis Belgium S.A., Beļģija
QI04AB01;QI02AB01
cattle; sheep
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for injection
International name (active substance):
Clostridium perfringens, epsilon-toxoid (type D), Clostridium perfringens, beta-toxoid (type B and C), Toxoid Clostridium novyi, Clostridium tetani toxoid, C. perfringens type A toxoid, C. chauvoei whole culture, C. septicum toxoid, C. sordellii toxoid, C. haemolyticum toxoid
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Pfizer Animal Health S.A., Beļģija
Date of authorisation/renewal:
23-Sep-2024
Marketing authorisation valid until:
22-Sep-2029
Marketing authorisation procedure:
I
Package leaflet:
[DOCX] 23092024_LI (23-Sep-2024)
Labelling text:
See products section
Summary of product characteristics:
-
Products
ID
Strength
Package size
Primary packaging
Labelling
V/I/24/0063-01
1
Polietilēna pudele, 100 ml
[PDF]
Baycox Iron
-
EU/2/19/239/001
Bayer Animal Health , Vācija
QP51BC51
pigs
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for injection
International name (active substance):
Toltrazuril, Iron III (as gleptoferron complex)
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Produlab Pharma b.v., Nīderlande
Date of authorisation/renewal:
20-May-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/2/19/239/001
36 mg/182 ml
1
Stikla flakons, 100 ml
-
Porcilis PCV M Hyo ID
-
EU/2/24/319/007
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/2/24/319/007
1
PET flakons, 200 deva
-
Felpreva
-
EU/2/21/277/011
Vetoquinol S.A., Francija
QP52AA51
cats
Vairāk
Medicinal product information
Pharmaceutical form:
spot-on solution
International name (active substance):
Tigolaner, Emodepside, Praziquantel
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Vetoquinol S.A., Francija
Date of authorisation/renewal:
11-Nov-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/2/21/277/011
10
Polipropilēna aplikators, 1,18 ml
-
Daxocox
45 mg
EU/2/21/270/046
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:
19-Dec-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/2/21/270/046
1
Blisteris, 5 tablete
-
Porcilis Lawsonia
-
V/I/23/0034
Intervet International B.V., Nīderlande
QI09AB18
pigs
Vairāk
Medicinal product information
Pharmaceutical form:
lyophilisate and solvent for emulsion for injection
International name (active substance):
Inactivated Lawsonia intracellularis strain SPAH-08
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Intervet International B.V., Nīderlande
Date of authorisation/renewal:
17-Jul-2023
Marketing authorisation valid until:
16-Jul-2028
Marketing authorisation procedure:
I
Package leaflet:
[DOCX] 26042024LI (26-Apr-2024)
Labelling text:
See products section
Summary of product characteristics:
-
Products
ID
Strength
Package size
Primary packaging
Labelling
V/I/23/0034-01
1
PET flakons, 50 devas/flakonā
[PDF]
[PDF]
[PDF]
V/I/23/0034-02
1
PET flakons, 100 devas/flakonā
[PDF]
[PDF]
[PDF]
UpCard
7.50 mg
EU/2/15/184/005
Vetoquinol S.A., Francija
QC03CA04
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
tablets
International name (active substance):
Torasemide
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Vetoquinol S.A., Francija
Date of authorisation/renewal:
24-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/2/15/184/005
7,5 mg
3
PVH/PHTFE alumīnija blisteris, 10 tablete
-
Fluralaner Intervet
100 mg
EU/2/25/346/007
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/2/25/346/007
3
Blisteris, 1 tablete
-
CANIVERM
-
V/I/19/0075
Bioveta a.s., Čehija
QP52AA51
dogs; cats; wolves; jackals; lions; hyenas
Vairāk
Medicinal product information
Pharmaceutical form:
tablets
International name (active substance):
Fenbendazole, Pyrantel embonate, Praziquantel
Distribution category:
Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release
Bioveta, a.s., Čehija
Date of authorisation/renewal:
02-Oct-2024
Marketing authorisation valid until:
01-Oct-2029
Marketing authorisation procedure:
I
Package leaflet:
[DOCX] 02102024_LI (02-Oct-2024)
Labelling text:
See products section
Summary of product characteristics:
-
Products
ID
Strength
Package size
Primary packaging
Labelling
V/I/19/0075-01
100
Blisteris, 1 tablete
[PDF]
Novem
40 mg/ml
EU/2/04/042/015
Boehringer Ingelheim Vetmedica GmbH, Vācija
QM01AC06
cattle
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:
02-Mar-2004
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/2/04/042/015
40 mg/ml
1
Stikla flakons, 50 ml
-
Zolvix
25 mg/ml
EU/2/09/101/004
Elanco GmbH, Vācija
QP52AX09
sheep
Vairāk
Medicinal product information
Pharmaceutical form:
solution for oral use
International name (active substance):
Monepantel
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:
03-Nov-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/2/09/101/004
25 mg/ml
1
Plastmasas pudele, 0,5 l
-
Bravecto
500 mg
EU/2/13/158/025
Intervet International B.V., Nīderlande
QP53B
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
spot-on solution
International name (active substance):
Fluralaner
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Intervet UK Ltd, Lielbritānija
Date of authorisation/renewal:
13-Feb-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/2/13/158/025
500 mg
2
Pipete, 1 deva
-