Veterinary medicinal product register

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Data selected by 2575
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
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 -
Credelio Plus - EU/2/21/271/019 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/2/21/271/019 1 Al/Al blisteris, 6 tablete -
Porcilis PCV - EU/2/08/091/003 Intervet International B.V., Nīderlande QI09AA07 pigs Vairāk

Medicinal product information

Pharmaceutical form: emulsion 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 Intervet International B.V., Nīderlande
Date of authorisation/renewal: 14-Jan-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/2/08/091/003 1 Pudelīte, 100 ml -

3081 record