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 4
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
Ezeepour 25 mg/ml V/NRP/08/1593 Bimeda Animal Health Limited, Īrija QP53AC08 cattle Vairāk

Medicinal product information

Pharmaceutical form: Pour-on solution
International name (active substance): Cypermethrin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bimeda Animal Health Limited, Īrija
Date of authorisation/renewal: 01-Jul-2013
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (26-May-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (26-May-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (26-May-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/08/1593-01 1 ABPE pudele, 500 ml -
V/NRP/08/1593-02 1 ABPE konteiners, 2500 ml -
Enroxil 50 mg/ml V/NRP/95/0195 KRKA, d.d., Novo mesto, Slovēnija QJ01MA90 cattle; pigs; sheep; goats; dogs; calves 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 KRKA, d.d., Novo mesto, Slovēnija
Date of authorisation/renewal: 16-Dec-2010
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (11-Oct-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (11-Oct-2023)
Summary of product characteristics: [PDF] Zāļu_informācija_ZA_M_LI (11-Oct-2023)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/95/0195-01 50 mg/ml 1 Stikla pudelīte (brūna), 50 ml -
V/NRP/95/0195-02 50 mg/ml 1 Stikla pudelīte (brūna), 100 ml -
Enroxil 100 mg/ml V/NRP/95/0194 KRKA, d.d., Novo mesto, Slovēnija 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 KRKA, d.d., Novo mesto, Slovēnija
Date of authorisation/renewal: 16-Dec-2010
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (11-Oct-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (11-Oct-2023)
Summary of product characteristics: [PDF] Zāļu_informācija_ZA_M_LI (11-Oct-2023)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/95/0194-01 100 mg/ml 1 Stikla pudelīte (brūna), 50 ml -
V/NRP/95/0194-02 100 mg/ml 1 Stikla pudelīte (brūna), 100 ml -
Enroxil 100 mg/ml V/NRP/96/0301 KRKA, d.d., Novo mesto, Slovēnija QJ01MA90 turkeys; chickens Vairāk

Medicinal product information

Pharmaceutical form: solution for oral use
International name (active substance): Enrofloxacin
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: 15-Oct-2010
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (01-Jul-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (01-Jul-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (01-Jul-2024)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/96/0301-01 100 mg/ml 1 Stikla pudelīte (brūna), 100 ml -
V/NRP/96/0301-02 100 mg/ml 1 Stikla pudelīte (brūna), 1 l -
Dalmazin SYNCH 0.075 mg/ml V/DCP/19/0078 Fatro S.p.A., Itālija QG02AD90 cattle; pigs; horses Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): D-cloprostenol
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Fatro S.p.A., Itālija
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 (31-Oct-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (31-Oct-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (31-Oct-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/19/0078-01 15 Stikla flakons, 2 ml -
V/DCP/19/0078-02 60 Stikla flakons, 2 ml -
V/DCP/19/0078-03 1 Stikla flakons, 10 ml -
V/DCP/19/0078-04 1 Stikla flakons, 20 ml -
V/DCP/19/0078-05 1 ABPE konteiners, 100 ml -
Bicormicina L.A. - V/NRP/02/1495 Fatro S.p.A., Itālija QJ01RV01 cattle; pigs; goats; horses; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Procaine benzylpenicillin, Benzathine benzylpenicillin, Dihydrostreptomycin sulphate, Dexamethasone sodium phosphate, Dexamethasone isonicotinate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Fatro S.p.A., Itālija
Date of authorisation/renewal: 15-Jul-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Jun-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Jun-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (16-Jun-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/02/1495-01 1 Stikla flakons, 100 ml -
V/NRP/02/1495-03 1 Stikla flakons, 50 ml -
Gentacin 100 mg/ml V/NRP/08/1585 Huvepharma EOOD, Bulgārija QJ01GB03 cattle; pigs; horses; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Gentamicin sulphate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Biovet Joint Stock Company, Bulgārija
Date of authorisation/renewal: 12-Apr-2013
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Jun-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Jun-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (06-Jun-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/08/1585-01 100 mg/ml 1 Stikla flakons, 50 ml -
V/NRP/08/1585-02 100 mg/ml 1 Stikla flakons, 100 ml -
Marbox 100 mg/ml V/DCP/10/0027 Ceva Sante Animale', Francija QJ01MA93 cattle; pigs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Marbofloxacin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Ceva Sante Animale., Francija
Date of authorisation/renewal: 04-Aug-2015
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (09-Apr-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (09-Apr-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (11-Jul-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/10/0027-01 100 mg/ml 1 Plastikāta pudelīte, 50 ml -
V/DCP/10/0027-02 100 mg/ml 1 Plastikāta pudelīte, 100 ml -
V/DCP/10/0027-03 100 mg/ml 1 Plastikāta pudelīte, 250 ml -
V/DCP/10/0027-04 100 mg/ml 1 Plastikāta pudelīte, 500 ml -
BioEquin FH - V/MRP/14/0070 Bioveta, a.s., Čehija QI05AA04 horses Vairāk

Medicinal product information

Pharmaceutical form: emulsion for injection
International name (active substance): Inactivated equine herpes virus type 1, Influenza A virus, subtype H3N8, strain A/equine/Brno/08, inactivated, Influenza A virus , subtype H3N8, strain A/equine/Limerick/2010, inactivated
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bioveta, a.s., Čehija
Date of authorisation/renewal: 02-Feb-2018
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Dec-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Dec-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (10-Dec-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/14/0070-01 2 Stikla flakons, 1 deva -
V/MRP/14/0070-02 5 Stikla flakons, 1 deva -
V/MRP/14/0070-03 10 Stikla flakons, 1 deva -
V/MRP/14/0070-04 1 Stikla flakons, 5 deva -
V/MRP/14/0070-05 10 Stikla flakons, 5 deva -
BioBos IBR marker live - V/MRP/17/0018 Bioveta, a.s., Čehija QI02AD01 cattle Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and solvent for suspension
International name (active substance): Live attenuated Bovine herpesvirus type 1 (BHV-1), strain Bio-27: IBR gE - negative
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bioveta, a.s., Čehija
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 (17-Dec-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Dec-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (01-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/17/0018-01 5 Stikla flakons, 5 deva -
V/MRP/17/0018-02 1 Stikla flakons, 25 deva -
LV Genta-100 100 mg/ml V/NRP/12/0045 Interchemie Werken De Adelaar Eesti AS, Igaunija QJ01GB03 cattle; pigs; sheep; goats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Gentamicin sulphate
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: 04-Jul-2017
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Jul-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Jul-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (03-Jul-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/12/0045-01 100 mg/ml 1 Stikla (tumša) flakons, 100 ml -
Primodog - V/NRP/96/0261 Boehringer Ingelheim Animal Health France SCS , Francija QI07AD01 dogs Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Canine parvovirus, strain Cornell 780916, Live
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: 16-Nov-2010
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (02-Jul-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (02-Jul-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (02-Jul-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/96/0261-01 10 Stikla flakons, 1 deva -
V/NRP/96/0261-02 50 Stikla flakons, 1 deva -
LV Interflox Oral 100 mg/ml V/NRP/11/0066 Interchemie Werken De Adelaar Eesti AS, Igaunija QJ01MA90 turkeys; chickens Vairāk

Medicinal product information

Pharmaceutical form: Solution for use in drinking water
International name (active substance): Enrofloxacin
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: 30-Nov-2016
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (25-Apr-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (25-Apr-2025)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (25-Apr-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/11/0066-01 100 mg/ml 1 ABPE pudele, 1000 ml -
V/NRP/11/0066-02 100 mg/ml 1 ABPE pudele, 100 ml -
V/NRP/11/0066-03 100 mg/ml 1 ABPE pudele, 500 ml -
Vetoryl 120 mg V/SRP/25/0028 Dechra Regulatory B.V., Nīderlande QH02CA01 dogs Vairāk

Medicinal product information

Pharmaceutical form: chewable tablets
International name (active substance): Trilostane
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 24-Apr-2025
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: SRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (24-Apr-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (24-Apr-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (24-Apr-2025)

Products

ID Strength Package size Primary packaging Labelling
V/SRP/25/0028-01 1 PA/Al/PVH blisteris, 10 tablete -
V/SRP/25/0028-02 3 PA/Al/PVH blisteris, 10 tablete -
V/SRP/25/0028-03 5 PA/Al/PVH blisteris, 10 tablete -
V/SRP/25/0028-04 6 PA/Al/PVH blisteris, 10 tablete -
V/SRP/25/0028-05 10 PA/Al/PVH blisteris, 10 tablete -
Amodip 1.25 mg V/DCP/15/0008 Ceva Sante Animale', Francija QC08CA01 cats Vairāk

Medicinal product information

Pharmaceutical form: chewable tablets
International name (active substance): Amlodipine
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release CEVA SANTE ANIMALE, Francija
Date of authorisation/renewal: 26-Feb-2020
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Feb-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Feb-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (11-Jul-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/15/0008-01 1,25 mg 3 Al/OPA/Al/PVH blisteris, 10 tablete -
V/DCP/15/0008-02 1,25 mg 10 Al/OPA/Al/PVH blisteris, 10 tablete -
V/DCP/15/0008-03 1,25 mg 20 Al/OPA/Al/PVH blisteris, 10 tablete -
Domitor Vet 1 mg/ml V/NRP/02/1453 Orion Corporation, Somija 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 Orion Corporation Orion Pharma, Somija
Date of authorisation/renewal: 16-Oct-2012
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Jan-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Jan-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (27-Jan-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/02/1453-01 1 mg/ml 1 Stikla flakons, 10 ml -
Frontline Combo Cat - V/NRP/03/1587 Boehringer Ingelheim Animal Health France SCS , Francija QP53AX65 ferrets; cats Vairāk

Medicinal product information

Pharmaceutical form: spot-on solution
International name (active substance): Fipronil,S-Methoprene
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release Boehringer Ingelheim Animal Health France SCS., Francija
Date of authorisation/renewal: 15-Jul-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (28-May-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (28-May-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (15-May-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/03/1587-01 1 Blisteris, 1 deva -
V/NRP/03/1587-02 3 Blisteris, 1 deva -
V/NRP/03/1587-03 6 Blisteris, 1 deva -
Colvasone 2 mg/ml V/NRP/98/0804 Norbrook Laboratories (Ireland) Limited, Īrija QH02AB02 cattle; horses; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Dexamethasone sodium phosphate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Norbrook Manufacturing Limited, Īrija
Date of authorisation/renewal: 08-Dec-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 31052019_LI (31-May-2019)
Labelling text: [PDF] 31052019_M (31-May-2019)
Summary of product characteristics: [PDF] 31052019_ZA (31-May-2019)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/98/0804-01 2 mg/ml 1 Flakons, 50 ml -
Zuritol 25 mg/ml V/DCP/12/0037 Laboratorios Calier, S.A., Spānija QP51BC01 chickens Vairāk

Medicinal product information

Pharmaceutical form: Solution for use in drinking water
International name (active substance): Toltrazuril
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Laboratorios Calier, S.A., Spānija
Date of authorisation/renewal: 28-Apr-2017
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (30-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (30-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (30-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/12/0037-01 25 mg/ml 1 Polietilēna pudelīte, 1 l -
V/DCP/12/0037-02 25 mg/ml 1 PE pudele ar PE vāciņu, 5 l -
Intraseal 2.6 g V/DCP/13/0029 Norbrook Laboratories (Ireland) Limited, Īrija QG52X cattle Vairāk

Medicinal product information

Pharmaceutical form: intramammary suspension
International name (active substance): Bismuth subnitrate
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release Norbrook Laboratories Limited, Lielbritānija;Norbrook Manufacturing Limited, Īrija
Date of authorisation/renewal: 28-Dec-2018
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (19-Nov-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (19-Nov-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (14-Feb-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/13/0029-01 2,6 g/deva 24 polietilēna šļirce, 1 deva -
V/DCP/13/0029-02 2,6 g/deva 60 polietilēna šļirce, 1 deva -
V/DCP/13/0029-03 2,6 g/deva 120 polietilēna šļirce, 1 deva -

3082 records