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
Prevestrus vet 100 mg/tabl. EU/2/25/338/012 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/2/25/338/012 1 ABPE burka, 28 tablete -
Trocoxil 30 mg EU/2/08/084/003 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/2/08/084/003 30 mg/tabl. 2 Alumīnija blisteris, 1 tablete [PDF]
Equilis Te - EU/2/05/055/001 Intervet International Booxmer, Nīderlande QI05AB03 horses Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Tetanus toxoid
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Intervet International Booxmer, Nīderlande
Date of authorisation/renewal: 12-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/2/05/055/001 10 Stikla flakons, 1 deva -
GUMBOHATCH - EU/2/19/245/004 Laboratorios Hipra S.A., Spānija QI01AD09 chickens; embryonated chicken eggs Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and solvent for suspension for injection
International name (active substance): Live attenuated infectious bursal disease virus (IBDV), strain 1052
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Laboratorios Hipra S.A., Spānija
Date of authorisation/renewal: 12-Nov-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/2/19/245/004 10 Stikla flakons, 4000 devas/flakonā -
APOQUEL 5.4 mg EU/2/13/154/022 Zoetis Belgium S.A., Beļģija QD11AH90 dogs Vairāk

Medicinal product information

Pharmaceutical form: film-coated tablets
International name (active substance): Oclacitinib
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Zoetis Belgium S.A., Beļģija;Pfizer Italia S.R.L., Itālija
Date of authorisation/renewal: 13-Dec-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/2/13/154/022 5,4 mg 2 Blisteris, 10 tablete -
Novem 20 mg/ml EU/2/04/042/013 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/2/04/042/013 20 mg/ml 12 Stikla flakons, 100 ml -
T61 1 ml V/I/26/0024 Intervet International GmbH, Vācija QN51AX50 guinea pigs; hamsters; cattle; pigs; horses; mouses; rats; dogs; cats; rabbits; minks; pigeons Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Embutramide, Mebezonium iodide, Tetracaine hydrohchloride
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Intervet International GmbH, Vācija
Date of authorisation/renewal: 13-May-2026
Marketing authorisation valid until: 12-May-2031
Marketing authorisation procedure: I
Package leaflet: [DOCX] 13052026LI (13-May-2026)
Labelling text: See products section
Summary of product characteristics: -

Products

ID Strength Package size Primary packaging Labelling
V/I/26/0024-01 1 Stikla pudele (dzintarkrāsas), 50 ml [PDF]
Melovem 15 mg/ml EU/2/09/098/009 Dopharma Research B.V., Nīderlande QM01AC06 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 Dopharma B.V., Nīderlande
Date of authorisation/renewal: 06-Jun-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/2/09/098/009 1 ABPE pudele, 250 ml -
Metricure 500 mg V/I/21/0069 Intervet Ireland Ltd, Īrija QG51AA05 cattle Vairāk

Medicinal product information

Pharmaceutical form: intrauterine suspension
International name (active substance): Cephapirin benzathine
Distribution category: -
Manufacturer(s) responsible for batch release Intervet International B.V., Nīderlande
Date of authorisation/renewal: 09-Nov-2021
Marketing authorisation valid until: 08-Nov-2026
Marketing authorisation procedure: I
Package leaflet: [DOCX] 09112021LI (09-Nov-2021)
Labelling text: See products section
Summary of product characteristics: -

Products

ID Strength Package size Primary packaging Labelling
V/I/21/0069-01 500 mg/deva 10 Šļirce, 1 deva -
Bovela - EU/2/14/176/011 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/2/14/176/011 6 Stikla flakons, 25 deva -
Profender spot-on solution for large cats - EU/2/05/054/016 Vetoquinol S.A., Francija QP52AA51 cats Vairāk

Medicinal product information

Pharmaceutical form: spot-on solution
International name (active substance): Praziquantel,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: 27-Jul-2005
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/2/05/054/016 40 Pipete, 1 deva -
NexGard Combo - EU/2/20/267/001 Boehringer Ingelheim Vetmedica GmbH, Vācija QP54AA54 cats < 2.5 kg Vairāk

Medicinal product information

Pharmaceutical form: spot-on solution
International name (active substance): Esafoxolaner, Eprinomectin, Praziquantel
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: 06-Jan-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/2/20/267/001 1 Aplikators, 0,3 ml -
Tulaven 100 mg/ml EU/2/20/251/005 Ceva Sante Animale,, Francija 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 Ceva Sante Animale,, 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/2/20/251/005 1 Plastmasas flakons, 500 ml -
ERAVAC - EU/2/16/199/001 Laboratorios Hipra S.A., Spānija QI08AA rabbits Vairāk

Medicinal product information

Pharmaceutical form: emulsion for injection
International name (active substance): Inactivated rabbit haemorrhagic disease virus
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Laboratorios Hipra S.A., Spānija
Date of authorisation/renewal: 16-Aug-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/2/16/199/001 1 Stikla flakons, 10 deva -
Inflacam 330.0 mg/deva EU/2/11/134/022 Chanelle Pharmaceuticals Manufacturing Ltd., Īrija QM01AC06 horses Vairāk

Medicinal product information

Pharmaceutical form: granules
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/2/11/134/022 20 Papīra/PE/Al folijas/PE paciņa, 1,5 g -
CircoMax - EU/2/21/281/001 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/2/21/281/001 1 ABPE flakons, 50 ml -
NexGard 68.0 mg/tabl. EU/2/13/159/007 Boehringer Ingelheim Vetmedica GmbH, Vācija QP53BE01 dogs Vairāk

Medicinal product information

Pharmaceutical form: chewable tablets
International name (active substance): Afoxolaner
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release MERIAL, Francija
Date of authorisation/renewal: 13-Jul-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/2/13/159/007 68 mg/tabl. 1 PVH/Aclar/Al blisteris, 1 tablete -
APOQUEL 3.6 mg/tabl. EU/2/13/154/011 Zoetis Belgium S.A., Beļģija QD11AH90 dogs Vairāk

Medicinal product information

Pharmaceutical form: film-coated tablets
International name (active substance): Oclacitinib
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Pfizer Italia S.R.L., Itālija
Date of authorisation/renewal: 26-Jul-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/2/13/154/011 3,6 mg/tabl. 1 ABPE pudelīte, 50 tablete -
TOLFENAMIC ACID VMD 40 mg/ml EU/2/24/329/003 V.M.D. n.v., Beļģija QM01AG02 cattle; pigs; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Tolfenamic acid
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release -
Date of authorisation/renewal: 03-Feb-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/2/24/329/003 1 Stikla flakons, 100 ml -
RESPIPORC FLU3 - EU/2/09/103/002 Ceva Sante Animale,, Francija QI09AA03 pigs Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Strains of inactivated Influenza A virus/ swine
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release IDT Biologika GmbH, Vācija
Date of authorisation/renewal: 13-Jan-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/2/09/103/002 1 Stikla flakons, 50 ml -

3081 record