Credelio
900 mg
EU/2/17/206/013
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/2/17/206/013
900 mg
1
Alumīnija blisteris, 1 deva
-
RESPIPORC FLUpan H1N1
-
EU/2/17/209/002
Ceva Sante Animale,, Francija
QI09AA03
pigs
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for injection
International name (active substance):
Inactivated influenza A virus/human, strain A/Jena/VI5258/2009(H1N1)pdm09
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
IDT Biologika GmbH, Vācija
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/2/17/209/002
1
Pudele, 50 deva
-
OSURNIA
-
EU/2/14/170/003
Dechra Regulatory B.V., Nīderlande
QS02CA90
dogs
Vairāk
Medicinal product information
Pharmaceutical form:
gel for local use
International name (active substance):
Betamethasone,Florfenicol,Betamethasone acetate,Terbinafine
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
GENERA Inc., Horvātija;Argenta Dundee Limited, Lielbritānija
Date of authorisation/renewal:
17-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/2/14/170/003
20
Tūbiņa, 2,05 g
-
Suvaxyn Circo
-
EU/2/17/223/003
Zoetis Belgium S.A., Beļģija
QI09AA
fattening pigs
Vairāk
Medicinal product information
Pharmaceutical form:
emulsion for injection
International name (active substance):
Inactivated porcine circovirus with type 2 ORF2 protein
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
-
Date of authorisation/renewal:
07-Feb-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/2/17/223/003
125 deva
1
Polietilēna flakons, 250 ml
-
Bovela
-
EU/2/14/176/015
Boehringer Ingelheim Vetmedica GmbH, Vācija
QI02AD02
cattle
Vairāk
Medicinal product information
Pharmaceutical form:
lyophilisate and solvent for suspension for injection
International name (active substance):
Modified live BVDV-1, non-cytopathic parent strain KE-9,Modified live bovine viral diarrhoea virus type 2, non-cytopathic parent strain NY-93
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Boehringer Ingelheim Animal Health USA Inc., ASV
Date of authorisation/renewal:
21-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/2/14/176/015
6
Stikla flakons, 50 deva
-
Ultifend ND IBD
-
EU/2/21/272/003
Ceva-Phylaxia Veterinary Biologicals Co. Ltd., Ungārija
QI01AD16
chickens; embryonated chicken eggs
Vairāk
Medicinal product information
Pharmaceutical form:
concentrate and solvent for suspension for injection
International name (active substance):
Cell-associated live recombinant turkey herpesvirus (rHVT/ND/IBD), expressing the fusion protein ofNewcastle disease virus and the VP2 protein of infectious bursal disease virus
Distribution category:
To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release
Ceva-Phylaxia Veterinary Biologicals Co. Ltd., Ungārija
Date of authorisation/renewal:
20-Apr-2021
Marketing authorisation valid until:
19-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/2/21/272/003
1
Stikla ampula, 4000 deva
-
MELOXIDYL
0.5 mg/ml
EU/2/06/070/010
Ceva Sante Animale., Francija
QM01AC06
cats
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/2/06/070/010
0,5 mg/ml
1
Stikla pudele, 5 ml
-
Cirbloc M Hyo
-
EU/2/24/322/004
Ceva-Phylaxia Veterinary Biologicals Co. Ltd., Ungārija
QI09AL08
fattening pigs
Vairāk
Medicinal product information
Pharmaceutical form:
emulsion for injection
International name (active substance):
Inactivated Mycoplasma hyopneumoniae, strain 2940
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/2/24/322/004
10
ZBPE pudele, 100 ml
-
Ingelvac CircoFLEX
-
EU/2/07/079/009
Boehringer Ingelheim Vetmedica GmbH, Vācija
QI09AA07
pigs
Vairāk
Medicinal product information
Pharmaceutical form:
suspension for injection
International name (active substance):
Inactivated recombinant Porcine Circovirus type 2
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Boehringer Ingelheim Vetmedica GmbH, Vācija
Date of authorisation/renewal:
13-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/2/07/079/009
1
TwistPak pudele, 10 ml
-
Imrestor
5.5 mg/ml
EU/2/15/193/001
Elanco GmbH, Vācija
QL03AA90
cattles (dairy cows)
Vairāk
Medicinal product information
Pharmaceutical form:
solution for injection
International name (active substance):
Pegbovigrastim (Pegylated bovine Granulocyte Colony Stimulating Factor)
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Eli Lilly and Company Ltd, Lielbritānija
Date of authorisation/renewal:
30-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/2/15/193/001
5,5 mg/ml
10
Polipropilēna pilnšļirce, 2,7 ml
-
Daxocox
15 mg
EU/2/21/270/001
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/2/21/270/001
15 mg
1
Blisteris, 4 tablete
-
PREVEXXION RN+HVT
0.2 ml
EU/2/23/302/002
Boehringer Ingelheim Vetmedica GmbH, Vācija
QI01AD03
chickens
Vairāk
Medicinal product information
Pharmaceutical form:
concentrate and solvent for suspension for injection
International name (active substance):
Cell-associated live recombinant Marek’s disease (MD) virus, serotype 1,strain RN1250, Cell-associated, live attenuated Marek’s disease (MD) virus, serotype 3,strain HVT FC126
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Boehringer Ingelheim Animal Health France SCS , Francija
Date of authorisation/renewal:
24-Oct-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/2/23/302/002
5
Stikla ampula, 2000 deva
-
Porcilis Porcoli Diluvac Forte
-
EU/2/96/001/003
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/2/96/001/003
1
Flakons, 20 ml
-
Mirataz
20 mg/g
EU/2/19/247/001
Dechra Regulatory B.V., Nīderlande
QN06AX11
cats
Vairāk
Medicinal product information
Pharmaceutical form:
ointment
International name (active substance):
Mirtazapine (as hemihydrate)
Distribution category:
To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release
Klifovet AG , 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/2/19/247/001
20 mg/g
1
Alumīnija tūbiņa (plastmasas pudelē), 5 g
-
Daxocox
200 mg
EU/2/21/270/040
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:
02-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/2/21/270/040
1
Blisteris, 4 tablete
-
Metacam
2 mg/ml
EU/2/97/004/039
Boehringer Ingelheim Vetmedica GmbH, Vācija
QM01AC06
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
Labiana Life Sciences S.A., Spānija
Date of authorisation/renewal:
01-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/2/97/004/039
2 mg/ml
1
Flakons, 10 ml
-
Advocate Spot-on šķīdums maziem suņiem
-
EU/2/03/039/041
Bayer Animal Health , Vācija
QP54AB52
small dogs
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:
16-Jul-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/2/03/039/041
9
Pipete, 0,4 ml
-
Loxicom
0.5 mg/ml
EU/2/08/090/027
Norbrook Laboratories (Ireland) Limited, Īrija
QM01AC06
cats
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
-
Date of authorisation/renewal:
12-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/2/08/090/027
0,5 mg/ml
1
Polietilēna pudele, 5 ml
-
Cirbloc M Hyo
-
EU/2/24/322/005
Ceva-Phylaxia Veterinary Biologicals Co. Ltd., Ungārija
QI09AL08
fattening pigs
Vairāk
Medicinal product information
Pharmaceutical form:
emulsion for injection
International name (active substance):
Inactivated Mycoplasma hyopneumoniae, strain 2940
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/2/24/322/005
48
ZBPE pudele, 100 ml
-
Advocate Spot-on šķīdums maziem suņiem
-
EU/2/03/039/015
Bayer Animal Health , Vācija
QP54AB52
dogs
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/2/03/039/015
4
Pipete, 0,4 ml
-