Veterinary medicinal product register

The FVS registers website is using cookies. By continuing using this website you are agreeing to use cookies. Agree Cookies policy
Data selected by 3003
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
Zuprevo 180 mg/ml EU/2/11/124/005 Intervet International B.V., Nīderlande QJ01FA96 cattle Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Tildipirosin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Intervet International GmbH, Vācija
Date of authorisation/renewal: 22-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/2/11/124/005 180 mg/ml 1 Flakons, 20 ml -
Procox - EU/2/11/123/002 Vetoquinol S.A., Francija QP52AX dogs Vairāk

Medicinal product information

Pharmaceutical form: suspension for oral use
International name (active substance): Toltrazuril,Emodepside
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: 14-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/2/11/123/002 1 Stikla pudelīte, 20 ml -
Inflacam 1.5 mg/ml EU/2/11/134/003 Chanelle Pharmaceuticals Manufacturing Ltd., Īrija 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 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/2/11/134/003 1,5 mg/ml 1 Pudelīte, 100 ml -
Tulissin 100 mg/ml EU/2/20/252/006 VIRBAC, Francija QJ01FA94 cattle 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 FAREVA AMBOISE, Francija;VIRBAC, Francija
Date of authorisation/renewal: 24-Apr-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/2/20/252/006 100 mg/ml 1 Stikla flakons, 500 ml -
Purevax RCP - EU/2/04/052/004 Boehringer Ingelheim Vetmedica GmbH, Vācija QI06AH09 cats Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and solvent for suspension for injection
International name (active substance): Attenuated feline rhinotracheitis herpesvirus,Live attenuated feline panleucopenia virus,Inactivated feline Calicivirosis antigens
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Merial Laboratory of Lyon Porte des Alpes, Francija
Date of authorisation/renewal: 25-Jan-2010
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/2/04/052/004 1 devas/flakonā 50 Pudele, 1 deva -
Bovilis Cryptium - EU/2/23/303/004 Intervet International B.V., Nīderlande QI02AO02 Cattle (pregnant heifer); Cattle (pregnant cow) Vairāk

Medicinal product information

Pharmaceutical form: emulsion for injection
International name (active substance): Cryptosporidium parvum, glycoprotein gp40
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release -
Date of authorisation/renewal: 23-Nov-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/2/23/303/004 1 Stikla flakons, 100 ml -
Trilorale 50 mg/ml EU/2/24/313/007 Axience, Francija QH02CA01 dogs Vairāk

Medicinal product information

Pharmaceutical form: Oral solution
International name (active substance): Trilostane
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release -
Date of authorisation/renewal: 06-May-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/2/24/313/007 50 mg/ml 1 Polipropilēna pudele, 72 ml -
Vaxxitek HVT+IBD+H5 - EU/2/25/354/001 Boehringer Ingelheim Vetmedica GmbH, Vācija QI01AD chickens; turkeys; embryonated chicken eggs Vairāk

Medicinal product information

Pharmaceutical form: concentrate and solvent for suspension for injection
International name (active substance): Turkey herpesvirus, strain rHVT-IBD-H5, expressing the VP2 protein gene of Infectious bursal disease virus and haemagglutinin gene of Avian influenza virus subtype H5, Live
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release -
Date of authorisation/renewal: 19-Nov-2025
Marketing authorisation valid until: 18-Nov-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/2/25/354/001 1 Stikla ampula, 2000 deva -
Emdocam 20 mg/ml EU/2/11/128/001 Emdoka bvba, 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 Produlab Pharma b.v., Nīderlande
Date of authorisation/renewal: 21-Jun-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/2/11/128/001 20 mg/ml 1 Pudelīte (caurspīdīga), 50 ml -
Parvoruvax - V/I/24/0071 Ceva Sante Animale', Francija QI09AL01 pigs Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Inactivated porcine parvovirus, Erysipelothrix rhusiopathiae
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: 26-Nov-2024
Marketing authorisation valid until: 25-Nov-2029
Marketing authorisation procedure: I
Package leaflet: [DOCX] 26082025LI (26-Aug-2025)
Labelling text: See products section
Summary of product characteristics: -

Products

ID Strength Package size Primary packaging Labelling
V/I/24/0071-01 1 Flakons, 25 deva [PDF] [PDF]
Zuprevo 180 mg/ml EU/2/11/124/008 Intervet International B.V., Nīderlande QJ01FA96 cattle Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Tildipirosin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Intervet International GmbH, Vācija
Date of authorisation/renewal: 22-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/2/11/124/008 180 mg/ml 1 Flakons, 250 ml -
Trocoxil 20 mg EU/2/08/084/002 Zoetis Belgium S.A., Beļģija QM01AH92 dogs Vairāk

Medicinal product information

Pharmaceutical form: chewable tablets
International name (active substance): Mavacoxib
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Pfizer (Heinrich Mack Nachf), Vācija
Date of authorisation/renewal: 22-Sep-2008
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/2/08/084/002 20 mg/tabl. 2 Alumīnija blisteris, 1 tablete -
Loxitab 1 mg EU/2/23/301/003 CP-Pharma Handelsgesellschaft GmbH, Vācija QM01AC06 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Meloxicam
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release -
Date of authorisation/renewal: 19-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/2/23/301/003 5 PVH/PE/PVDH-Al blisteris, 10 tablete -
Loxicom 0.5 mg/ml EU/2/08/090/009 Norbrook Laboratories (Ireland) Limited, Īrija 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 Norbrook Laboratories Limited, Lielbritānija
Date of authorisation/renewal: 12-Mar-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/2/08/090/009 0,5 mg/ml 1 Polietilēna pudele, 15 ml -
Prevestrus vet 25 mg/tabl. EU/2/25/338/001 Vetcare Oy, Somija - dogs (bitches) Vairāk

Medicinal product information

Pharmaceutical form: film-coated tablets
International name (active substance): Finrozole
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release -
Date of authorisation/renewal: 23-Apr-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/2/25/338/001 1 Blisteris, 7 tablete -
Emepax 24 mg 24 mg EU/2/26/363/003 Axience, Francija QA04AD90 dogs Vairāk

Medicinal product information

Pharmaceutical form: chewable tablets
International name (active substance): Maropitant citrate monohydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 26-Mar-2026
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/2/26/363/003 3 OPA/Al/PVH-Al blisteris, 4 tablete -
Nobilis IB 4 - 91 - EU/2/98/006/018 Intervet International Booxmer, Nīderlande QI01AD07 chickens Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate for suspension
International name (active substance): Live attenuated Infectious Bronchitis virus
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release -
Date of authorisation/renewal: 21-May-2008
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/2/98/006/018 12 Polipropilēna trauciņš, 10000 deva -
Bovela - EU/2/14/176/016 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/2/14/176/016 10 Stikla flakons, 50 deva -
Chanhold 360 mg EU/2/19/236/016 Chanelle Pharmaceuticals Manufacturing Ltd., Īrija QP54AA05 dogs 40,1–60,0 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/2/19/236/016 120 mg/ml 6 Plastmasas pipete, 3 ml -
RESPIVAC TRT - EU/2/24/314/006 Laboratorios Hipra S.A., Spānija QI01AD01 chickens Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate for oculonasal suspension/use in drinking water
International name (active substance): Turkey rhinotracheitis virus, strain 1062, Live
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release -
Date of authorisation/renewal: 30-May-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/2/24/314/006 10 Stikla flakons, 2000 devas/flakonā -

3081 record