Veterinary medicinal product register

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Data selected by 554
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
AVITUBAL 28 000 28000 IU/ml V/NRP/01/1331 Bioveta, a.s., Čehija QV04CF01 chickens Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Mycobacterium avium, subsp. avium, strain D4ER, avian tuberculin protein derivative
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bioveta, a.s., Čehija
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 (18-May-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (18-May-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (18-May-2026)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/01/1331-02 28000 IU/ml 5 Stikla flakons, 10 ml -
V/NRP/01/1331-03 28000 IU/ml 10 Stikla flakons, 5 ml [DOCX] [DOCX] [DOCX]
Quiflox 80 mg V/DCP/12/0075 KRKA, d.d., Novo mesto, Slovēnija QJ01MA93 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Marbofloxacin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release KRKA, d.d., Novo mesto, Slovēnija;TAD Pharma GmbH, Vācija
Date of authorisation/renewal: 03-Jan-2018
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (11-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (11-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (11-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/12/0075-01 80 mg 2 OPA/Al/PVH-Al blisteris, 6 tablete -
V/DCP/12/0075-02 80 mg 12 OPA/Al/PVH-Al blisteris, 6 tablete -
Vey Tosal - V/DCP/23/0031 Veyx-Pharma GmbH, Vācija QA12CX99 cattle; horses; dogs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): BUTAFOSFAN, Cyanocobalamin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Veyx-Pharma GmbH, Vācija;Veyx-Pharma B.V., Nīderlande
Date of authorisation/renewal: 27-Jun-2023
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Mar-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Mar-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (12-Aug-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/23/0031-01 100 ml 1 Stikla pudele (dzintarkrāsas), 100 ml [PDF] [PDF]
V/DCP/23/0031-02 250 ml 1 Stikla pudelīte (dzintarkrāsas), 250 ml [PDF] [PDF]
Killitam Drops 15 mg/ml V/NRP/02/1492 Fatro S.p.A., Itālija QN05AA04 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: drops for oral use
International name (active substance): Acepromazine maleate
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: [DOC] Skat_sadaļā_Zāļu_apraksts (16-Oct-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Oct-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (16-Oct-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/02/1492-01 15 mg/ml 1 Flakons, 20 ml -
Killitam Tablets 10 mg V/NRP/02/1491 Fatro S.p.A., Itālija QN05AA04 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Acepromazine maleate
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-Oct-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Oct-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (16-Oct-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/02/1491-01 10 mg 1 Blisteris, 10 tablete -
V/NRP/02/1491-02 10 mg 2 Blisteris, 10 tablete -
Triderm - V/DCP/19/0020 Organit Kft., Ungārija QD06C dogs Vairāk

Medicinal product information

Pharmaceutical form: cutaneous spray, solution
International name (active substance): Prednisolone,Marbofloxacin,Ketoconazole
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Alphavet Zrt, Ungārija
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 01092025LI (01-Sep-2025)
Labelling text: [PDF] 02052019M (02-May-2019)
Summary of product characteristics: [DOC] 02052019ZA (18-Dec-2020)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/19/0020-01 1 PET pudele, 30 ml -
Kiltix 3,02 g + 0,68 g - V/NRP/25/0045 Elanco Animal Health GmbH, Vācija QP53AC55 dogs Vairāk

Medicinal product information

Pharmaceutical form: medicated collar
International name (active substance): Flumethrin, Propoxur (2-isopropoxyphenyl- methylcarbamate)
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release KVP Pharma + Veterinar Produkte GmbH, Vācija
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 (07-Jul-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (07-Jul-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (07-Jul-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/25/0045-01 1 Poliestera/polietilēna/alumīnija maisiņš, 30,2 g -
Kiltix 4,5 g + 1,013 g - V/NRP/25/0046 Elanco Animal Health GmbH, Vācija QP53AC55 dogs Vairāk

Medicinal product information

Pharmaceutical form: medicated collar
International name (active substance): Flumethrin, Propoxur (2-isopropoxyphenyl- methylcarbamate)
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release KVP Pharma + Veterinar Produkte GmbH, Vācija
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 (07-Jul-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (07-Jul-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (07-Jul-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/25/0046-01 1 Poliestera/polietilēna/alumīnija maisiņš, 45 g -
Kiltix 1,25 g + 0,28 g - V/NRP/96/0416 Elanco Animal Health GmbH, Vācija QP53AC55 dogs Vairāk

Medicinal product information

Pharmaceutical form: medicated collar
International name (active substance): Flumethrin, Propoxur (2-isopropoxyphenyl- methylcarbamate)
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release KVP Pharma + Veterinar Produkte GmbH, Vācija
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 (07-Jul-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (07-Jul-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (07-Jul-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/96/0416-01 1 Poliestera/polietilēna/alumīnija maisiņš, 12,5 g -
NOVOSOL 500000 IU/g V/DCP/25/0061 Huvepharma NV, Beļģija QA07AA01 quails; cattle; pigs; ducks; turkeys; gooses; chickens; Partridge Vairāk

Medicinal product information

Pharmaceutical form: powder for use in drinking water/ milk
International name (active substance): Neomycin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release HUVEPHARMA SA, Francija
Date of authorisation/renewal: 08-Sep-2025
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (08-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (08-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (08-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/25/0061-01 1 Paciņa, 100 g -
V/DCP/25/0061-02 1 Maiss, 1 kg -
Perlutex 5 mg V/NRP/96/0296 Dechra Veterinary Products A/S, Dānija QG03DA02 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Medroxyprogesterone acetate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Haupt Pharma Münster GmbH, Vācija
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 (01-Jul-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (01-Jul-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (01-Jul-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/96/0296-01 5 mg 1 PVH/Al blisteris, 20 tablete -
V/NRP/96/0296-02 5 mg 1 PVH/Al blisteris, 60 tablete -
Canergy 100 mg V/DCP/15/0040 Le Vet Beheer B.V., Nīderlande QC04AD90 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Propentofylline
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande;Artesan Pharma, Vācija;GENERA Inc., Horvātija
Date of authorisation/renewal: 28-Apr-2020
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (13-May-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (13-May-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (13-May-2026)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/15/0040-01 100 mg 1 PA/Al/PVH//Al blisteris, 10 tablete -
V/DCP/15/0040-02 100 mg 2 PA/Al/PVH//Al blisteris, 10 tablete -
V/DCP/15/0040-03 100 mg 3 PA/Al/PVH//Al blisteris, 10 tablete -
V/DCP/15/0040-04 100 mg 4 PA/Al/PVH//Al blisteris, 10 tablete -
V/DCP/15/0040-05 100 mg 5 PA/Al/PVH//Al blisteris, 10 tablete -
V/DCP/15/0040-06 100 mg 6 PA/Al/PVH//Al blisteris, 10 tablete -
V/DCP/15/0040-07 100 mg 7 PA/Al/PVH//Al blisteris, 10 tablete -
V/DCP/15/0040-08 100 mg 8 PA/Al/PVH//Al blisteris, 10 tablete -
V/DCP/15/0040-09 100 mg 9 PA/Al/PVH//Al blisteris, 10 tablete -
V/DCP/15/0040-10 100 mg 10 PA/Al/PVH//Al blisteris, 10 tablete -
V/DCP/15/0040-11 100 mg 25 PA/Al/PVH//Al blisteris, 10 tablete -
V/DCP/15/0040-12 100 mg 50 PA/Al/PVH//Al blisteris, 10 tablete -
ISOFLUTEK 1000 mg/g V/MRP/22/0004 LABORATORIOS KARIZOO, S.A., Spānija QN01AB06 ferrets; guinea pigs; hamsters; chinchilla; horses; mouses; rats; dogs; cats; exotic birds; reptiles; gerbils Vairāk

Medicinal product information

Pharmaceutical form: inhalation vapour, liquid
International name (active substance): Isoflurane
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Laboratorios Karizoo S.A., Spānija
Date of authorisation/renewal: 27-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (22-Apr-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (22-Apr-2026)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (22-Apr-2026)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/22/0004-01 1000 mg/g 1 Stikla pudele (dzintarkrāsas), 250 ml -
Albiotic - V/NRP/03/0226 Huvepharma NV, Beļģija QJ51RF03 cattle (lactating cows) Vairāk

Medicinal product information

Pharmaceutical form: intramammary solution
International name (active substance): Neomycin, Lincomycin hydrohloride
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Biovet Joint Stock Company., Bulgārija
Date of authorisation/renewal: 21-May-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (13-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (13-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (13-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/03/0226-01 24 Injektors, 10 ml -
Firodyl 250 mg V/DCP/20/0003 Ceva Sante Animale', Francija QM01AH90 dogs Vairāk

Medicinal product information

Pharmaceutical form: chewable tablets
International name (active substance): Firocoxib
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release CEVA SANTE ANIMALE, Francija
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 (10-Oct-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Oct-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (10-Oct-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/20/0003-01 250 mg 2 PA/Al/PVH//Al blisteris, 6 tablete -
V/DCP/20/0003-02 250 mg 6 PA/Al/PVH//Al blisteris, 6 tablete -
V/DCP/20/0003-03 250 mg 16 PA/Al/PVH//Al blisteris, 6 tablete -
V/DCP/20/0003-04 250 mg 20 PA/Al/PVH//Al blisteris, 6 tablete -
Protivity - V/SRP/25/0064 Zoetis Belgium S.A., Beļģija QI02AE05 cattle Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and solvent for suspension for injection
International name (active substance): Mycoplasma bovis, strain N2805-1, Live
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Zoetis Belgium S.A., Beļģija
Date of authorisation/renewal: 15-Oct-2025
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: SRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (15-Oct-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (15-Oct-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (15-Oct-2025)

Products

ID Strength Package size Primary packaging Labelling
V/SRP/25/0064-01 1 Stikla flakons, 10 deva -
Calciject 40 CM - V/NRP/97/0576 Norbrook Laboratories (Ireland) Limited, Īrija QA12AX cattle Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Boric Acid, Calcium gluconate, Magnesium hypophosphite hexahydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Norbrook Manufacturing Limited, Īrija
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 (08-Dec-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (08-Dec-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (08-Dec-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/97/0576-01 1 Stikla flakons, 400 ml -
V/NRP/97/0576-02 1 Polipropilēna flakons, 400 ml -
Cloteid 4 - V/NRP/20/0024 Bioveta, ,a.s., Čehija QI05AB cattle; sheep; goats; horses; dogs Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Tetanus toxoid
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release Bioveta, a.s., Čehija
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [DOCX] 23102020LI (23-Oct-2020)
Labelling text: [DOCX] 23102020M (23-Oct-2020)
Summary of product characteristics: [DOCX] 23102020ZA (23-Oct-2020)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/20/0024-01 2 Stikla flakons, 1 ml -
V/NRP/20/0024-02 10 Stikla flakons, 1 ml -
V/NRP/20/0024-03 20 Stikla flakons, 1 ml -
V/NRP/20/0024-04 1 Stikla flakons, 5 ml -
V/NRP/20/0024-05 10 Stikla flakons, 5 ml -
LV Calmasol-204 S - V/NRP/19/0002 Interchemie Werken De Adelaar Eesti AS, Igaunija 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 Interchemie Werken De Adelaar Eesti AS, Igaunija
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 (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/NRP/19/0002-01 1 Polipropilēna flakons, 500 ml -
Propomitor 10 mg/ml V/DCP/20/0019 Orion Corporation, Somija QN01AX10 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: emulsion for injection/infusion
International name (active substance): Propofol
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release Orion Corporation Orion Pharma, Somija;Orion Corporation Orion Pharma,, Somija
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 (16-Nov-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Nov-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (16-Nov-2023)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/20/0019-01 10 mg/ml 1 Stikla flakons, 20 ml -
V/DCP/20/0019-02 10 mg/ml 1 Stikla flakons, 50 ml -
V/DCP/20/0019-03 10 mg/ml 1 Stikla flakons, 100 ml -
V/DCP/20/0019-04 10 mg/ml 5 Stikla flakons, 20 ml -

3082 records

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