Veterinary medicinal product register

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Data selected by 2
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
Porcilis PCV M Hyo ID - EU/2/24/319/008 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/2/24/319/008 10 PET flakons, 200 deva -
Chanhold 60 mg EU/2/19/236/006 Chanelle Pharmaceuticals Manufacturing Ltd., Īrija QP54AA05 cats 7,6 - 10,0 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/2/19/236/006 60 mg/ml 6 Plastmasas pipete, 1 ml -
Zuprevo 180 mg/ml EU/2/11/124/006 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/2/11/124/006 180 mg/ml 1 Flakons, 50 ml -
Innovax-ND-IBD-ILT - EU/2/25/347/001 Intervet International B.V., Nīderlande - chickens; embryonated chicken eggs Vairāk

Medicinal product information

Pharmaceutical form: concentrate and solvent for suspension for injection
International name (active substance): Turkey herpesvirus, strain HVT/ND/IBD/ILT, expressing fusion protein gene of NDV and VP2 protein gene of IBD virus and gD and gI glycoproteins genes of ILT virus, Live
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release -
Date of authorisation/renewal: 04-Jul-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/2/25/347/001 1 Stikla ampula, 2000 deva -
Stronghold 120 mg EU/2/99/014/010 Zoetis Belgium S.A., Beļģija QP54AA05 dogs 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 Pfizer Service Company bvba, Beļģija
Date of authorisation/renewal: 01-Oct-2009
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/2/99/014/010 120 mg/deva 6 Polipropilēna pudelīte, 1 deva -
Advocate Spot-on lieliem kaķiem - EU/2/03/039/037 Bayer Animal Health , Vācija QP54AB52 cats 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/2/03/039/037 9 Pipete, 0,8 ml -
Porcilis ColiClos - EU/2/12/141/008 Intervet International B.V., Nīderlande QI09AB08 pigs Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): F4ab (K88ab) fimbrial adhesin,F5 (K99) fimbrial adhesin,F4ac (K88ac) fimbrial adhesin,F6 (987P) fimbrial adhesin,Echerichia coli LT toxoid,Toxoid Clostridium perfringens, type C
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release -
Date of authorisation/renewal: 14-Jun-2012
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/2/12/141/008 100 deva 1 Stikla pudelīte, 100 deva -
CircoMax - EU/2/21/281/006 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/2/21/281/006 4 ABPE flakons, 250 ml -
Rabitec - EU/2/17/219/002 Ceva Sante Animale,, Francija QI07BD raccoon dogs; foxes Vairāk

Medicinal product information

Pharmaceutical form: suspension for oral use
International name (active substance): Attenuated live rabies virus
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release -
Date of authorisation/renewal: 07-Oct-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/2/17/219/002 4 Polimēra maiss, 200 deva -
Prid Delta - V/I/19/0049 Ceva Sante Animale,, Francija QG03DA04 cattle Vairāk

Medicinal product information

Pharmaceutical form: vaginal delivery system
International name (active substance): Progesterone
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Ceva Sante Animale, Francija
Date of authorisation/renewal: 20-Aug-2024
Marketing authorisation valid until: 19-Aug-2029
Marketing authorisation procedure: I
Package leaflet: [DOCX] 20082024LI (24-Apr-2026)
Labelling text: See products section
Summary of product characteristics: -

Products

ID Strength Package size Primary packaging Labelling
V/I/19/0049-01 1,55 g 10 Polietilēna maisiņš, 1 deva [PDF] [PDF]
Porcilis Glässer - V/I/23/0033 Intervet International B.V., Nīderlande QI09AB07 pigs Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Inactivated Haemophilus parasuis strain 4800
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Intervet International Booxmer, Nīderlande
Date of authorisation/renewal: 17-Jul-2023
Marketing authorisation valid until: 16-Jul-2028
Marketing authorisation procedure: I
Package leaflet: [DOCX] 26032025_LI (26-Mar-2025)
Labelling text: See products section
Summary of product characteristics: -

Products

ID Strength Package size Primary packaging Labelling
V/I/23/0033-01 1 Polietilēna pudelīte, 25 deva [PDF]
MELOXIDYL 20 mg/ml EU/2/06/070/005 Ceva Sante Animale., Francija 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 Ceva Sante Animale, Francija;Vetem SpA, Itālija
Date of authorisation/renewal: 25-Mar-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/2/06/070/005 20 mg/ml 1 Flakons, 50 ml -
Eurican Herpes 205 - EU/2/01/029/003 Boehringer Ingelheim Vetmedica GmbH, Vācija QI07AA06 dogs Vairāk

Medicinal product information

Pharmaceutical form: powder and solvent for emulsion for injection
International name (active substance): Canine herpesvirus antigen
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release MERIAL Laboratoire Porte des Alpes, Francija
Date of authorisation/renewal: 18-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/2/01/029/003 2 Stikla pudelīte, 1 deva -
Daxocox 140 mg EU/2/21/270/039 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/2/21/270/039 4 Blisteris, 5 tablete -
Nobilis Multriva Gm+REOm - EU/2/25/344/002 Intervet International B.V., Nīderlande QI01AA22 chickens Vairāk

Medicinal product information

Pharmaceutical form: emulsion for injection
International name (active substance): Infectious bursal disease virus, strain GB02, Inactivated
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release -
Date of authorisation/renewal: 02-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/2/25/344/002 1 PET pudele, 600 ml -
Imrestor 5.5 mg/ml EU/2/15/193/003 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/2/15/193/003 5,5 mg/ml 100 Polipropilēna šļirce, 2,7 ml -
Novem 20 mg/ml EU/2/04/042/006 Boehringer Ingelheim Vetmedica GmbH, Vācija QM01AC06 cattle; pigs 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: 13-Jan-2009
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/2/04/042/006 20 mg/ml 1 Stikla flakons, 250 ml -
OSURNIA - EU/2/14/170/001 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/2/14/170/001 2 Tūbiņa, 2,05 g -
Vectra 3D - EU/2/13/156/027 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/2/13/156/027 24 Polipropilēna aplikators, 1 deva -
Inflacam 2.5 mg EU/2/11/134/013 Chanelle Pharmaceuticals Manufacturing Ltd., Īrija QM01AC06 dogs Vairāk

Medicinal product information

Pharmaceutical form: chewable tablets
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/2/11/134/013 2,5 mg 1 Blisteris, 20 tablete -

3082 records