Veterinary medicinal product register

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Data selected by 391
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
Medeson 1 mg/ml V/MRP/15/0059 Industrial Veterinaria, S.A., Spānija QN05CM91 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Medetomidine hydrohloride
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release Industrial Veterinaria, S.A., Spānija
Date of authorisation/renewal: 23-Nov-2020
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (18-Jul-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (18-Jul-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (18-Jul-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/15/0059-01 1 mg/ml 1 Stikla flakons, 10 ml -
V/MRP/15/0059-02 1 mg/ml 6 Stikla flakons, 10 ml -
V/MRP/15/0059-03 1 mg/ml 5 Stikla flakons, 10 ml -
Dorbene vet 1 mg/ml V/MRP/11/0054 LABORATORIOS SYVA S.A., Spānija QN05CM91 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Medetomidine hydrohloride
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Laboratorios Syva S.A., Spānija
Date of authorisation/renewal: 16-Oct-2012
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (28-Jul-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (28-Jul-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (28-Jul-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/11/0054-01 1 mg/g 1 Stikla flakons, 10 ml -
Bioestrovet Swine 0.0875 mg/ml V/DCP/22/0027 Vetoquinol S.A., Francija QG02AD90 pigs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Cloprostenol sodium
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Vetoquinol S.A., Francija
Date of authorisation/renewal: 28-Jun-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (28-Jul-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (28-Jul-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (28-Jul-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/22/0027-01 0,0875 mg/ml 1 Stikla flakons, 20 ml -
V/DCP/22/0027-02 0,0875 mg/ml 1 Stikla flakons, 50 ml -
Tolfine 80 mg/ml V/DCP/22/0038 Vetoquinol S.A., Francija QM01AG02 cattle 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 Vetoquinol S.A., Francija
Date of authorisation/renewal: 28-Sep-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (01-Aug-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (01-Aug-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (01-Aug-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/22/0038-01 80 mg/ml 1 Stikla flakons, 50 ml -
V/DCP/22/0038-02 80 mg/ml 1 Stikla flakons, 100 ml -
V/DCP/22/0038-03 80 mg/ml 1 Stikla flakons, 250 ml -
Danilon Equidos 1.5 g V/DCP/11/0050 ECUPHAR VETERINARIA S.L.U, Spānija QM01AA90 horses; ponies Vairāk

Medicinal product information

Pharmaceutical form: granules
International name (active substance): Suxibuzone
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Laboratorios Dr.Esteve S.A, Spānija
Date of authorisation/renewal: 03-May-2016
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (07-Aug-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (07-Aug-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (07-Aug-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/11/0050-01 150 mg/g 18 Al/PE paciņa, 10 g -
V/DCP/11/0050-02 150 mg/g 60 Al/PE paciņa, 10 g -
Stromease 25 mg/ml V/DCP/21/0046 DOMES PHARMA, Francija QS01XA08 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: eye drops, solution
International name (active substance): Acetylcysteine
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release -
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (18-Aug-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (18-Aug-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (18-Aug-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/21/0046-01 25 mg/ml 1 Stikla pudele (dzintarkrāsas), 5 ml -
Emdofluxin 50 mg/ml V/DCP/20/0036 Emdoka bvba, Beļģija QM01AG90 cattle; pigs; horses Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Flunixin meglumine
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Produlab Pharma b.v., Nīderlande
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (01-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (01-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (01-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/20/0036-01 50 mg/ml 1 Stikla flakons, 50 ml -
V/DCP/20/0036-02 50 mg/ml 1 Stikla flakons, 100 ml -
V/DCP/20/0036-03 50 mg/ml 1 Stikla flakons, 250 ml -
Citramox 1000 mg/g V/MRP/20/0018 LABORATORIOS KARIZOO, S.A., Spānija QJ01CA04 pigs; ducks; turkeys; chickens Vairāk

Medicinal product information

Pharmaceutical form: powder for use in drinking water
International name (active substance): Amoxicillin trihydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release LABORATORIOS KARIZOO, S.A., Spānija
Date of authorisation/renewal: 21-May-2021
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (01-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (01-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (01-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/20/0018-01 1000 mg/g 1 Maiss, 200 g -
V/MRP/20/0018-02 1000 mg/g 1 Maiss, 500 g -
V/MRP/20/0018-03 1000 mg/g 1 Maiss, 1 kg -
V/MRP/20/0018-04 1000 mg/g 20 Maiss, 200 g -
Glucosol 400 mg/ml V/NRP/18/0026 Bela-pharm GmbH&Co.KG, Vācija QB05BA03 cattle; sheep Vairāk

Medicinal product information

Pharmaceutical form: solution for infusion
International name (active substance): Glucose monohydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bela-pharm GmbH&Co.KG, Vācija
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (05-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (05-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (05-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/18/0026-01 400 mg/1 ml 1 Polipropilēna flakons, 500 ml -
V/NRP/18/0026-02 400 mg/1 ml 12 Polipropilēna flakons, 500 ml -
V/NRP/18/0026-03 400 mg/1 ml 1 Polipropilēna flakons, 750 ml -
V/NRP/18/0026-04 400 mg/1 ml 12 Polipropilēna flakons, 750 ml -
Selectan 300 mg/ml V/MRP/11/0048 Laboratorios Hipra S.A., Spānija QJ01BA90 cattle; pigs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Florfenicol
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-Oct-2012
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (23-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (23-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (23-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/11/0048-01 300 mg/ml 1 Stikla pudele, 100 ml -
V/MRP/11/0048-02 300 mg/ml 1 PET pudele, 250 ml -
V/MRP/11/0048-03 300 mg/ml 10 Stikla pudele, 100 ml -
V/MRP/11/0048-04 300 mg/ml 10 PET pudele, 250 ml -
V/MRP/11/0048-05 300 mg/ml 12 PET pudele, 100 ml -
V/MRP/11/0048-06 300 mg/ml 12 PET pudele, 250 ml -
V/MRP/11/0048-07 300 mg/ml 1 PET pudele, 50 ml -
V/MRP/11/0048-08 300 mg/ml 1 PET pudele, 100 ml -
V/MRP/11/0048-09 300 mg/ml 10 PET pudele, 100 ml -
V/MRP/11/0048-10 300 mg/ml 12 Stikla pudele, 100 ml -
Roxacin 100 mg/ml V/NRP/01/1292 Laboratorios Calier, S.A., Spānija QJ01MA90 cattle; pigs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Enrofloxacin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Laboratorios Calier, S.A., Spānija
Date of authorisation/renewal: 13-Jun-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (23-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (23-Sep-2025)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (23-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/01/1292-01 100 mg/ml 1 Flakons, 100 ml -
V/NRP/01/1292-02 100 mg/ml 1 Flakons, 250 ml -
Oxy-200 LA 200 mg/ml V/NRP/15/0047 Interchemie Werken De Adelaar Eesti AS, Igaunija QJ01AA06 cattle; pigs; sheep; goats; turkeys; chickens Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Oxytetracycline dihydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Interchemie Werken De Adelaar Eesti AS, Igaunija
Date of authorisation/renewal: 01-Jul-2020
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (22-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (22-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (22-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/15/0047-01 200 mg/ml 1 Stikla pudele, 100 ml -
Rycarfa Flavour 50 mg V/DCP/10/0017 KRKA, d.d., Novo mesto, Slovēnija QM01AE91 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Carprofen
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release KRKA, d.d., Novo mesto, Slovēnija
Date of authorisation/renewal: 01-Jul-2015
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (17-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/10/0017-01 50 mg 2 Al/OPA/Al/PVH blisteris, 10 tablete -
V/DCP/10/0017-02 50 mg 5 Al/OPA/Al/PVH blisteris, 10 tablete [JPG] [JPG]
V/DCP/10/0017-03 50 mg 10 Al/OPA/Al/PVH blisteris, 10 tablete -
V/DCP/10/0017-04 50 mg 50 Al/OPA/Al/PVH blisteris, 10 tablete -
Rycarfa Flavour 20 mg V/DCP/10/0016 KRKA, d.d., Novo mesto, Slovēnija QM01AE91 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Carprofen
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release KRKA, d.d., Novo mesto, Slovēnija
Date of authorisation/renewal: 01-Jul-2015
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (17-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/10/0016-01 20 mg 2 Al/OPA/Al/PVH blisteris, 10 tablete -
V/DCP/10/0016-02 20 mg 5 Al/OPA/Al/PVH blisteris, 10 tablete -
V/DCP/10/0016-03 20 mg 10 Al/OPA/Al/PVH blisteris, 10 tablete -
V/DCP/10/0016-04 20 mg 50 Al/OPA/Al/PVH blisteris, 10 tablete -
Rycarfa Flavour 100 mg V/DCP/10/0018 KRKA, d.d., Novo mesto, Slovēnija QM01AE91 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Carprofen
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release KRKA, d.d., Novo mesto, Slovēnija;Virbac S.A., Francija
Date of authorisation/renewal: 01-Jul-2015
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (17-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/10/0018-01 100 mg 2 Al/OPA/Al/PVH blisteris, 10 tablete -
V/DCP/10/0018-02 100 mg 5 Al/OPA/Al/PVH blisteris, 10 tablete -
V/DCP/10/0018-03 100 mg 10 Al/OPA/Al/PVH blisteris, 10 tablete -
V/DCP/10/0018-04 100 mg 50 Al/OPA/Al/PVH blisteris, 10 tablete -
Neoskilab 1.5 mg V/DCP/21/0039 Labiana Life Sciences S.A., Spānija QN07AA01 cattle; sheep; goats; horses Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Neostigmine methylsulfate
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: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 30062021LI (30-Jun-2021)
Labelling text: [DOCX] 30062021M (30-Jun-2021)
Summary of product characteristics: [DOCX] 30062021ZA (30-Jun-2021)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/21/0039-01 1,5 mg/ml 1 Flakons, 25 ml -
Tramvetol 50 mg/ml V/DCP/19/0071 VIRBAC, Francija QN02AX02 dogs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Tramadol hydrochloride
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release Labiana Life Sciences S.A., Spānija
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] 30102019LI (30-Oct-2019)
Labelling text: [PDF] 30102019M (30-Oct-2019)
Summary of product characteristics: [PDF] 30102019ZA (30-Oct-2019)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/19/0071-01 50 mg/ml 10 Stikla ampula, 1 ml -
Solamocta 697 mg/g V/MRP/18/0023 Eurovet Animal Health B.V., Nīderlande QJ01CA04 ducks; turkeys; chickens Vairāk

Medicinal product information

Pharmaceutical form: Powder for use in drinking water
International name (active substance): Amoxicillin trihydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Eurovet Animal Health B.V., Nīderlande
Date of authorisation/renewal: 21-Sep-2020
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (21-Feb-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (21-Feb-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (21-Feb-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/18/0023-01 1 Paciņa, 100 g -
V/MRP/18/0023-02 1 Paciņa, 250 g -
V/MRP/18/0023-03 1 Paciņa, 500 g -
V/MRP/18/0023-04 1 Paciņa, 1 kg -
V/MRP/18/0023-05 1 PET/AL/PE maisiņš, 100 g -
V/MRP/18/0023-06 1 PET/AL/PE maisiņš, 250 g -
V/MRP/18/0023-07 1 PET/AL/PE maisiņš, 500 g -
V/MRP/18/0023-08 1 PET/AL/PE maisiņš, 1 kg -
Octacillin 800 mg/g V/MRP/21/0038 Eurovet Animal Health B.V., Nīderlande QJ01CA04 pigs Vairāk

Medicinal product information

Pharmaceutical form: Powder for use in drinking water
International name (active substance): Amoxicillin trihydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Eurovet Animal Health B.V., Nīderlande
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (02-Jun-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (02-Jun-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (02-Jun-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/21/0038-01 800 mg/g 1 Maisiņš (no ārpuses balts slānis), 100 g -
V/MRP/21/0038-02 800 mg/g 1 Maisiņš (no ārpuses balts slānis), 250 g -
V/MRP/21/0038-03 800 mg/g 1 Maisiņš (no ārpuses balts slānis), 500 g -
V/MRP/21/0038-04 800 mg/g 1 Maisiņš (no ārpuses balts slānis), 1 kg -
V/MRP/21/0038-05 800 mg/g 1 Maisiņš (no ārpuses poliestera slānis), 100 g -
V/MRP/21/0038-06 800 mg/g 1 Maisiņš (no ārpuses poliestera slānis), 250 g -
V/MRP/21/0038-07 800 mg/g 1 Maisiņš (no ārpuses poliestera slānis), 500 g -
V/MRP/21/0038-08 800 mg/g 1 Maisiņš (no ārpuses poliestera slānis), 1 kg -
Mexxam Vet 0.5 mg/ml V/DCP/24/0033 Alfasan Nederland BV, Nīderlande QM01AC06 guinea pigs; 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 Produlab Pharma b.v., Nīderlande;Alfasan Nederland BV, Nīderlande
Date of authorisation/renewal: 16-May-2024
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (16-May-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (16-May-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (16-May-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/24/0033-01 1 ABPE pudelīte, 5 ml -
V/DCP/24/0033-02 1 ABPE pudelīte, 10 ml -
V/DCP/24/0033-03 1 ABPE pudelīte, 25 ml -

3082 records