Veterinary medicinal product register

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Data selected by 792
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
LV Intracox Oral 25 mg/ml V/NRP/11/0067 Interchemie Werken De Adelaar Eesti AS, Igaunija QP51AJ01 turkeys; chickens Vairāk

Medicinal product information

Pharmaceutical form: solution for oral use
International name (active substance): Toltrazuril
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: [DOCX] 23012023LI (23-Jan-2023)
Labelling text: [DOCX] 23012023M (23-Jan-2023)
Summary of product characteristics: [DOCX] 23012023ZA (23-Jan-2023)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/11/0067-01 25 mg/ml 1 ABPE pudele, 1000 ml -
V/NRP/11/0067-02 25 mg/ml 1 ABPE pudele, 100 ml -
V/NRP/11/0067-03 25 mg/ml 1 ABPE pudele, 500 ml -
Calci-kel 300 - V/NRP/00/1229 Kela Laboratoria NV, Beļģija QA12AX cattle; sheep Vairāk

Medicinal product information

Pharmaceutical form: solution for infusion
International name (active substance): Calcium gluconate,Magnesium chloride
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Kela Laboratoria NV, Beļģija
Date of authorisation/renewal: 05-Jul-2012
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Jul-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Jul-2024)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (03-Jul-2024)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/00/1229-01 1 Polipropilēna pudele, 500 ml -
Feligen CRP - V/NRP/08/1606 Virbac S.A., Francija QI06AD04 cats Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and solvent for suspension for injection
International name (active substance): Live feline calicivirus, strain F9,Live rhinotracheitis virus F2 strain,Live Panleucopenia virus LR72 strain
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Virbac S.A., Francija
Date of authorisation/renewal: 30-May-2013
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (29-Jul-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (29-Jul-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (29-Jul-2024)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/08/1606-01 50 Stikla flakons, 1 deva -
V/NRP/08/1606-02 10 Stikla flakons, 1 deva -
Apiguard 250 mg/g V/NRP/03/1594 Vita Bee Health Limited, Īrija QP53AX22 bees Vairāk

Medicinal product information

Pharmaceutical form: gel for beehive use
International name (active substance): Thymol
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release CICIEFFE S.R.L., Itālija
Date of authorisation/renewal: 22-Sep-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Jun-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Jun-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (10-Jun-2024)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/03/1594-01 250 mg/g 10 Folijas paciņa, 50 g -
Calcio PH - V/NRP/01/1377 Fatro S.p.A., Itālija QA12AX cattle; pigs; sheep; horses; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Calcium gluconate, Toldimfos sodium, Magnesium chloride hexahydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Fatro S.p.A., Itālija
Date of authorisation/renewal: 04-Jul-2011
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Nov-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Nov-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (26-Nov-2024)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/01/1377-01 1 Stikla flakons, 250 ml -
V/NRP/01/1377-02 1 Stikla flakons, 500 ml -
Metabolase Forte - V/NRP/02/1494 Fatro S.p.A., Itālija QA11JC00 cattle; pigs; sheep; horses Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): A-tocopherol acetate,D-L Acetylmethionine,L-carnitine hydrochloride,Cyanocobalamin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Fatro S.p.A., Itālija
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 (02-Dec-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (02-Dec-2024)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (02-Dec-2024)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/02/1494-01 1 Flakons, 100 ml -
V/NRP/02/1494-02 1 Flakons, 250 ml -
Frontline Spray 2.5 mg/ml V/NRP/95/0160 Boehringer Ingelheim Animal Health France SCS , Francija QP53AX15 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: cutaneous spray, solution
International name (active substance): Fipronil
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release Boehringer Ingelheim Animal Health France SCS., Francija
Date of authorisation/renewal: 03-Aug-2010
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [DOCX] 280720LI (28-Jul-2020)
Labelling text: [DOCX] 280720M (28-Jul-2020)
Summary of product characteristics: [DOCX] 280720ZA (28-Jul-2020)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/95/0160-01 2,5 mg/ml 1 Flakons, 100 ml -
V/NRP/95/0160-02 2,5 mg/ml 1 Flakons, 250 ml -
V/NRP/95/0160-03 2,5 mg/ml 1 Flakons, 500 ml -
Decomoton 0.05 mg/ml V/NRP/01/1293 Laboratorios Calier, S.A., Spānija QH01BB03 cattle; pigs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Carbetocin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Laboratorios Calier, S.A., Spānija
Date of authorisation/renewal: 31-Jan-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (08-Aug-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (08-Aug-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (08-Aug-2024)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/01/1293-01 0,05 mg/ml 1 Stikla flakons, 10 ml -
Bovilis BVD - V/NRP/02/1524 Intervet International BV, Nīderlande QI02AA01 cattle Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Cytopathogenic Bovine Viral Diarrhoea virus
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Intervet International Booxmer, Nīderlande
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 (27-Dec-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Dec-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (27-Dec-2023)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/02/1524-02 1 Stikla flakons, 10 ml -
V/NRP/02/1524-03 1 Stikla flakons, 20 ml -
V/NRP/02/1524-04 1 Stikla flakons, 50 ml -
V/NRP/02/1524-05 1 Stikla flakons, 250 ml -
V/NRP/02/1524-06 1 Stikla flakons, 100 ml -
V/NRP/02/1524-07 1 PET flakons, 10 ml -
V/NRP/02/1524-08 1 PET flakons, 20 ml -
V/NRP/02/1524-09 1 PET flakons, 50 ml -
V/NRP/02/1524-10 1 PET flakons, 100 ml -
V/NRP/02/1524-11 1 PET flakons, 250 ml -
Spasmipur 20 mg/ml V/DCP/19/0017 VetViva Richter GmbH , Austrija QA03BB01 cattle; pigs; sheep; horses Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Hyoscine butylbromide
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release VetViva Richter GmbH , Austrija
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 (06-Nov-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Nov-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (06-Nov-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/19/0017-01 1 Stikla flakons, 50 ml -
Menbutil 100 mg/ml V/DCP/18/0062 aniMedica GmbH, Vācija QA05AX90 cattle; pigs; sheep; goats; horses Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Menbutone
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release aniMedica GmbH, Vācija;Industrial Veterinaria, S.A., Spānija
Date of authorisation/renewal: 27-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Dec-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Dec-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (16-Dec-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/18/0062-01 100 mg/ml 1 Stikla flakons, 100 ml -
V/DCP/18/0062-02 100 mg/ml 12 Stikla flakons, 100 ml -
Fipron 67 mg V/MRP/16/0021 Bioveta, a.s., Čehija QP53AX15 small dogs

Medicinal product information

Pharmaceutical form: spot-on solution
International name (active substance): Fipronil
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release Bioveta, a.s., Čehija
Date of authorisation/renewal: 01-Feb-2017
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] 300117LI (01-Feb-2017)
Labelling text: [PDF] 300117M (01-Feb-2017)
Summary of product characteristics: [PDF] 300117ZA (01-Feb-2017)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/16/0021-01 67 mg/deva 1 Polietilēna tūbiņa, 1 deva -
V/MRP/16/0021-02 67 mg/deva 3 Polietilēna tūbiņa, 1 deva -
V/MRP/16/0021-03 67 mg/deva 25 Polietilēna tūbiņa, 1 deva -
Fipron 134 mg V/MRP/16/0022 Bioveta, a.s., Čehija QP53AX15 medium dogs Vairāk

Medicinal product information

Pharmaceutical form: spot-on solution
International name (active substance): Fipronil
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release Bioveta, a.s., Čehija
Date of authorisation/renewal: 01-Feb-2017
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] 300117LI (01-Feb-2017)
Labelling text: [PDF] 300117M (01-Feb-2017)
Summary of product characteristics: [PDF] 300117ZA (01-Feb-2017)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/16/0022-01 134 mg/deva 1 Polietilēna tūbiņa, 1 deva -
V/MRP/16/0022-02 134 mg/deva 3 Polietilēna tūbiņa, 1 deva -
V/MRP/16/0022-03 134 mg/deva 25 Polietilēna tūbiņa, 1 deva -
Thoro VAX vet. - V/MRP/05/1662 Intervet International B.V., Nīderlande QI09AB13 pigs Vairāk

Medicinal product information

Pharmaceutical form: emulsion for injection
International name (active substance): Inactivated Mycoplasma hyopneumoniae
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release Burgwedel Biotech GmbH, Vācija
Date of authorisation/renewal: 23-Aug-2007
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [DOC] 280324LI (28-Mar-2024)
Labelling text: [PDF] 191214M (22-Dec-2014)
Summary of product characteristics: [DOCX] 191214ZA (22-Dec-2014)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/05/1662-01 1 Polietilēna pudele, 50 deva -
V/MRP/05/1662-02 2 Polietilēna pudele, 50 deva -
V/MRP/05/1662-03 5 Polietilēna pudele, 50 deva -
V/MRP/05/1662-04 10 Polietilēna pudele, 50 deva -
V/MRP/05/1662-05 1 Polietilēna pudele, 100 deva -
V/MRP/05/1662-06 2 Polietilēna pudele, 100 deva -
V/MRP/05/1662-07 5 Polietilēna pudele, 100 deva -
V/MRP/05/1662-08 10 Polietilēna pudele, 100 deva -
V/MRP/05/1662-09 1 Polietilēna pudele, 200 deva -
V/MRP/05/1662-10 2 Polietilēna pudele, 200 deva -
V/MRP/05/1662-11 5 Polietilēna pudele, 200 deva -
V/MRP/05/1662-12 10 Polietilēna pudele, 200 deva -
Canigen DHPPi/L - V/MRP/15/0057 VIRBAC, Francija QI07AI02 dogs Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and suspension for suspension for injection
International name (active substance): Canine distemper virus, Lederle strain, Canine parvovirus, C.P.V.780916 strain, Canine parainfluenza virus, Manhattan strain, Live attenuated Canine Adenovirus type 2 (CAV2), strain Manhattan, Inactivated Leptospira canicola, Inactivated Leptospira icterohaemorrhagiae
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release VIRBAC, Francija
Date of authorisation/renewal: 29-Jul-2020
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Jan-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Jan-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (26-Jan-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/15/0057-01 1 Stikla flakons, 1 deva -
V/MRP/15/0057-02 10 Stikla flakons, 1 deva -
V/MRP/15/0057-03 25 Stikla flakons, 1 deva -
V/MRP/15/0057-04 50 Stikla flakons, 1 deva -
V/MRP/15/0057-05 100 Stikla flakons, 1 deva -
Calciveyxol 38 - V/NRP/00/1250 Veyx-Pharma GmbH, Vācija QA12AX cattle; pigs; sheep Vairāk

Medicinal product information

Pharmaceutical form: solution for infusion
International name (active substance): Calcii gluconas monohydricus, Magnesii chloridum hexahydricum, Acidum boricum
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Veyx-Pharma GmbH, Vācija
Date of authorisation/renewal: 08-Jun-2010
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [DOCX] 180520LI (18-May-2020)
Labelling text: [DOCX] 180520M (18-May-2020)
Summary of product characteristics: [DOCX] 180520ZA (18-May-2020)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/00/1250-01 1 Plastmasas flakons, 500 ml -
V/NRP/00/1250-02 12 Polietilēna flakons, 500 ml -
V/NRP/00/1250-03 6 Polietilēna flakons, 500 ml -
Tenazym - V/NRP/99/1034 Veyx-Pharma GmbH, Vācija QJ01RV01 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: suspension for oral use
International name (active substance): Trypsin,Neomycin sulphate,Papain,Chymotrypsin,Prednisolone acetate,Tetracycline hydrochloridum
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Veyx-Pharma B.V., Nīderlande
Date of authorisation/renewal: 07-Aug-2009
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 09112018LI (09-Nov-2018)
Labelling text: [PDF] 09112018M (09-Nov-2018)
Summary of product characteristics: [PDF] 09112018ZA (09-Nov-2018)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/99/1034-01 10 Injektors, 10 ml -
Cefaximin-L - V/NRP/01/1376 Fatro S.p.A., Itālija QJ51RD34 lactating cows Vairāk

Medicinal product information

Pharmaceutical form: intramammary suspension
International name (active substance): Rifaximin, Cephacetrile sodium
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Fatro S.p.A., Itālija
Date of authorisation/renewal: 04-Jul-2011
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Mar-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Mar-2025)
Summary of product characteristics: [DOCX] ZA_M_LI (27-Mar-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/01/1376-01 4 Injektors, 1 deva -
V/NRP/01/1376-02 12 Injektors, 1 deva -
Opticlox eye ointment 167 mg/g V/NRP/98/0813 Norbrook Laboratories (Ireland) Limited, Īrija QS01AA90 cattle; sheep; horses; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: eye ointment
International name (active substance): Cloxacillin benzathine
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Norbrook Laboratories Limited, Lielbritānija;Norbrook Manufacturing Limited, Īrija
Date of authorisation/renewal: 22-Oct-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 310519LI (31-May-2019)
Labelling text: [PDF] 310519M (31-May-2019)
Summary of product characteristics: [PDF] 310519ZA (31-May-2019)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/98/0813-01 167 mg/g 4 Polipropilēna šļirce, 5 g -
Drycloxa-kel 685,13 mg/9 g - V/NRP/98/0717 Kela Laboratoria NV, Beļģija QJ51CF02 cattle Vairāk

Medicinal product information

Pharmaceutical form: intramammary suspension
International name (active substance): Cloxacillin benzathine
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Kela Laboratoria NV, Beļģija
Date of authorisation/renewal: 15-Jul-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 040419LI (04-Apr-2019)
Labelling text: [PDF] 040419M (04-Apr-2019)
Summary of product characteristics: [PDF] 040419ZA (04-Apr-2019)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/98/0717-01 20 Injektors, 1 deva -

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