Veterinary medicinal product register

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Data selected by 209
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
Cevac MD HVT - V/DCP/16/0037 Ceva-Phylaxia Co.Ltd., Ungārija QI01AD03 chickens Vairāk

Medicinal product information

Pharmaceutical form: suspension and diluent for suspension for injection
International name (active substance): Live Turkey Herpes virus
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release Ceva-Phylaxia Veterinary Biologicals Co. Ltd., Ungārija
Date of authorisation/renewal: 29-Nov-2021
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 26112021LI (26-Nov-2021)
Labelling text: [DOCX] 26112021M (26-Nov-2021)
Summary of product characteristics: [DOCX] 26112021ZA (26-Nov-2021)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/16/0037-01 1 Ampula, 500 deva -
V/DCP/16/0037-02 1 Ampula, 1000 deva -
V/DCP/16/0037-03 1 Ampula, 2000 deva -
V/DCP/16/0037-04 1 Ampula, 4000 deva -
V/DCP/16/0037-05 1 Maiss (šķīdinātājs), 200 ml -
V/DCP/16/0037-06 1 Maiss (šķīdinātājs), 400 ml -
V/DCP/16/0037-07 1 Maiss (šķīdinātājs), 800 ml -
V/DCP/16/0037-08 1 Maiss (šķīdinātājs), 1000 ml -
V/DCP/16/0037-09 1 Maiss (šķīdinātājs), 1200 ml -
V/DCP/16/0037-10 1 Maiss (šķīdinātājs), 1600 ml -
Ingelvac Ery emulsija injekcijām cūkām - V/DCP/21/0030 Boehringer Ingelheim Vetmedica GmbH, Vācija QI09AB03 pigs Vairāk

Medicinal product information

Pharmaceutical form: emulsion for injection
International name (active substance): Erysipelothrix rhusiopathiae, serotype 2, strain SE-9, Inactivated
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release LABORATORIOS SYVA, S.A.U. , Spānija
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 08042024_LI (08-Apr-2024)
Labelling text: [DOCX] 19122022_M (19-Dec-2022)
Summary of product characteristics: [DOCX] 19122022_ZA (19-Dec-2022)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/21/0030-01 1 Polipropilēna flakons, 100 ml -
Thyrovet 800 µg V/DCP/24/0008 CP-Pharma Handelsgesellschaft GmbH, Vācija QH03AA01 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Levothyroxine sodium
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release CP-Pharma Handelsgesellschaft GmbH, Vācija
Date of authorisation/renewal: 12-Jan-2024
Marketing authorisation valid until: 11-Jan-2029
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (12-Jan-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (12-Jan-2024)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (28-Feb-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/24/0008-01 800 µg/tabl. 3 AL/PVC-AL-PA blisteris, 10 tablete -
V/DCP/24/0008-02 800 µg/tabl. 10 AL/PVC-AL-PA blisteris, 10 tablete -
Rodotium 162 mg/ml V/MRP/24/0022 Huvepharma EOOD, Bulgārija QJ01XQ01 pigs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Tiamulin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Biovet AD, Bulgārija
Date of authorisation/renewal: 07-Mar-2024
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (07-Mar-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (07-Mar-2024)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (07-Mar-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/24/0022-01 1 Stikla pudele, 100 ml -
Equisedan 10 mg/ml V/MRP/13/0033 Vetcare Oy, Somija QN05CM90 horses Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Detomidine hydrochloride
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release Laboratorios SYVA S.A.U, Spānija;Tairgi Tread-Lia Baile na Sceilge Teo (Trading as Ballinskelligs Veterinary Products), Īrija
Date of authorisation/renewal: 30-Oct-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Mar-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Mar-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (26-Mar-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/13/0033-01 10 mg/ml 1 Stikla flakons, 10 ml -
V/MRP/13/0033-02 10 mg/ml 1 Stikla flakons, 15 ml -
Equibactin vet. - V/DCP/19/0040 Dechra Regulatory B.V., Nīderlande QJ01EW10 horses Vairāk

Medicinal product information

Pharmaceutical form: oral powder
International name (active substance): Sulfadiazine, Trimethoprim
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] 02082019LI (02-Aug-2019)
Labelling text: [PDF] 02082019M (02-Aug-2019)
Summary of product characteristics: [PDF] 02082019ZA (02-Aug-2019)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/19/0040-01 250/50 mg 1 ABPE trauciņš, 105 g -
V/DCP/19/0040-02 250/50 mg 1 ABPE trauciņš, 210 g -
V/DCP/19/0040-03 250/50 mg 1 ABPE trauciņš, 420 g -
V/DCP/19/0040-04 250/50 mg 1 Polipropilēna trauciņš, 840 g -
V/DCP/19/0040-05 250/50 mg 10 PET/AL/PE maisiņš, 5 g -
V/DCP/19/0040-06 250/50 mg 20 PET/AL/PE maisiņš, 5 g -
V/DCP/19/0040-07 250/50 mg 28 PET/AL/PE maisiņš, 5 g -
V/DCP/19/0040-08 250/50 mg 10 PET/AL/PE maisiņš, 15 g -
V/DCP/19/0040-09 250/50 mg 20 PET/AL/PE maisiņš, 15 g -
V/DCP/19/0040-10 250/50 mg 28 PET/AL/PE maisiņš, 15 g -
V/DCP/19/0040-12 250/50 mg 10 PET/AL/PE maisiņš, 30 g -
V/DCP/19/0040-13 250/50 mg 20 PET/AL/PE maisiņš, 30 g -
V/DCP/19/0040-14 250/50 mg 28 PET/AL/PE maisiņš, 30 g -
V/DCP/19/0040-16 250/50 mg 10 PET/AL/PE maisiņš, 60 g -
V/DCP/19/0040-17 250/50 mg 20 PET/AL/PE maisiņš, 60 g -
V/DCP/19/0040-18 250/50 mg 28 PET/AL/PE maisiņš, 60 g -
V/DCP/19/0040-20 250/50 mg 10 PET/AL/PE maisiņš, 100 g -
Versiguard Rabies - V/MRP/06/1668 Zoetis Belgium S.A., Beļģija QI07AA02 ferrets; cattle; pigs; sheep; goats; horses; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Inactivated Rabies virus
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bioveta, a.s., Čehija
Date of authorisation/renewal: 21-Mar-2011
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Sep-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Sep-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (20-Sep-2023)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/06/1668-01 10 Flakons, 1 deva -
V/MRP/06/1668-12 10 Flakons, 10 deva -
V/MRP/06/1668-16 1 Flakons, 1 deva -
Lineomam LC - V/MRP/17/0024 Bioveta, a.s., Čehija QJ51RF03 cattle (lactating cows) Vairāk

Medicinal product information

Pharmaceutical form: intramammary solution
International name (active substance): Lincomycin hydrohloride, Neomycin sulphate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bioveta, a.s., Čehija
Date of authorisation/renewal: 24-Feb-2021
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [DOCX] 230221LI (24-Feb-2021)
Labelling text: [DOCX] 230221M (24-Feb-2021)
Summary of product characteristics: [DOCX] 300523ZA (31-May-2023)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/17/0024-01 24 Injektors, 10 ml -
Profexx 50 mg/ml V/DCP/24/0025 Alfasan Nederland BV, Nīderlande QM01AE91 cattle Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Carprofen
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Alfasan Nederland BV, Nīderlande
Date of authorisation/renewal: 26-Mar-2024
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Mar-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Mar-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (26-Mar-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/24/0025-01 1 Stikla flakons, 50 ml -
V/DCP/24/0025-02 1 Stikla flakons, 100 ml -
V/DCP/24/0025-03 1 Stikla flakons, 250 ml -
Cartaxx 50 mg/ml V/DCP/24/0026 Alfasan Nederland BV, Nīderlande QM01AE91 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Carprofen
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Alfasan Nederland BV, Nīderlande
Date of authorisation/renewal: 26-Mar-2024
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Mar-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Mar-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (26-Mar-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/24/0026-01 1 Stikla flakons, 10 ml -
V/DCP/24/0026-02 1 Stikla flakons, 20 ml -
V/DCP/24/0026-03 1 Stikla flakons, 50 ml -
Nobivac Tricat Trio - V/MRP/07/1709 Intervet International B.V., Nīderlande QI06AD04 cats Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and solvent for suspension for injection
International name (active substance): Live attenuated feline rhinotracheitis virus, strain G2620A,Live, attenuated feline calici virus,Live attenuated feline panleucopenia virus
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Intervet International B.V., Nīderlande
Date of authorisation/renewal: 07-Oct-2011
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (24-Jan-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (24-Jan-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (24-Jan-2023)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/07/1709-01 5 Stikla flakons (kartona kastē), 1 deva -
V/MRP/07/1709-02 10 Stikla flakons (kartona kastē), 1 deva -
V/MRP/07/1709-03 25 Stikla flakons (kartona kastē), 1 deva -
V/MRP/07/1709-04 50 Stikla flakons (kartona kastē), 1 deva -
V/MRP/07/1709-05 5 Stikla flakons (plastikāta kastē), 1 deva -
V/MRP/07/1709-06 10 Stikla flakons (plastikāta kastē), 1 deva -
V/MRP/07/1709-07 25 Stikla flakons (plastikāta kastē), 1 deva -
V/MRP/07/1709-08 50 Stikla flakons (plastikāta kastē), 1 deva -
Nobivac Pi - V/MRP/22/0003 Intervet International B.V., Nīderlande QI07AD08 dogs Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and solvent for suspension for injection
International name (active substance): Canine parainfluenza virus, strain Cornell, Live
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Intervet International 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 (21-Jan-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (21-Jan-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (21-Jan-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/22/0003-01 5 Stikla flakons, 1 deva -
V/MRP/22/0003-02 10 Stikla flakons, 1 deva -
V/MRP/22/0003-03 25 Stikla flakons, 1 deva -
V/MRP/22/0003-04 50 Stikla flakons, 1 deva -
Oxytocin 10 IU/ml 10 IU/ml V/NRP/96/0314 Bela-pharm GmbH&Co.KG, Vācija QH01BB02 cattle; pigs; sheep; goats; horses; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Oxytocin
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: 07-Oct-2011
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (23-Feb-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (23-Feb-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (23-Feb-2026)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/96/0314-01 16,6 µg/ml 1 Stikla flakons, 10 ml -
V/NRP/96/0314-02 16,6 µg/ml 1 Stikla flakons, 50 ml -
V/NRP/96/0314-03 16,6 µg/ml 1 Stikla flakons, 100 ml -
V/NRP/96/0314-04 16,6 µg/ml 5 Stikla flakons, 10 ml -
V/NRP/96/0314-05 16,6 µg/ml 6 Stikla flakons, 10 ml -
V/NRP/96/0314-06 16,6 µg/ml 10 Stikla flakons, 10 ml -
V/NRP/96/0314-07 16,6 µg/ml 12 Stikla flakons, 10 ml -
V/NRP/96/0314-08 16,6 µg/ml 6 Stikla flakons, 50 ml -
V/NRP/96/0314-09 16,6 µg/ml 12 Stikla flakons, 50 ml -
V/NRP/96/0314-10 16,6 µg/ml 6 Stikla flakons, 100 ml -
V/NRP/96/0314-11 16,6 µg/ml 12 Stikla flakons, 100 ml -
Alpramil mg V/DCP/22/0018 Alfasan Nederland BV, Nīderlande QP54AB51 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): MILBEMYCINE OXIME, Praziquantel
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 27-May-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (09-Jan-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (09-Jan-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (09-Jan-2026)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/22/0018-01 1 Al/OPA/Al/PVH blisteris, 1 tablete -
V/DCP/22/0018-02 1 Al/OPA/Al/PVH blisteris, 2 tablete -
V/DCP/22/0018-03 1 Al/OPA/Al/PVH blisteris, 4 tablete -
V/DCP/22/0018-04 10 Al/OPA/Al/PVH blisteris, 1 tablete -
V/DCP/22/0018-05 10 Al/OPA/Al/PVH blisteris, 2 tablete -
V/DCP/22/0018-06 10 Al/OPA/Al/PVH blisteris, 4 tablete -
V/DCP/22/0018-07 25 Al/OPA/Al/PVH blisteris, 1 tablete -
V/DCP/22/0018-08 25 Al/OPA/Al/PVH blisteris, 2 tablete -
V/DCP/22/0018-09 25 Al/OPA/Al/PVH blisteris, 4 tablete -
Alpramil mg V/DCP/22/0019 Alfasan Nederland BV, Nīderlande QP54AB51 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): MILBEMYCINE OXIME, Praziquantel
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 27-May-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (09-Jan-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (09-Jan-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (09-Jan-2026)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/22/0019-01 1 Al/OPA/Al/PVH blisteris, 1 tablete -
V/DCP/22/0019-02 1 Al/OPA/Al/PVH blisteris, 2 tablete -
V/DCP/22/0019-03 1 Al/OPA/Al/PVH blisteris, 4 tablete -
V/DCP/22/0019-04 10 Al/OPA/Al/PVH blisteris, 1 tablete -
V/DCP/22/0019-05 10 Al/OPA/Al/PVH blisteris, 2 tablete -
V/DCP/22/0019-06 10 Al/OPA/Al/PVH blisteris, 4 tablete -
V/DCP/22/0019-07 25 Al/OPA/Al/PVH blisteris, 1 tablete -
V/DCP/22/0019-08 25 Al/OPA/Al/PVH blisteris, 2 tablete -
V/DCP/22/0019-09 25 Al/OPA/Al/PVH blisteris, 4 tablete -
Alpramil mg V/DCP/22/0020 Alfasan Nederland BV, Nīderlande QP54AB51 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): MILBEMYCINE OXIME, Praziquantel
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 27-May-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (09-Jan-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (09-Jan-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (09-Jan-2026)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/22/0020-01 1 Al/OPA/Al/PVH blisteris, 1 tablete -
V/DCP/22/0020-02 1 Al/OPA/Al/PVH blisteris, 2 tablete -
V/DCP/22/0020-03 1 Al/OPA/Al/PVH blisteris, 4 tablete -
V/DCP/22/0020-04 10 Al/OPA/Al/PVH blisteris, 1 tablete -
V/DCP/22/0020-05 10 Al/OPA/Al/PVH blisteris, 2 tablete -
V/DCP/22/0020-06 10 Al/OPA/Al/PVH blisteris, 4 tablete -
V/DCP/22/0020-07 25 Al/OPA/Al/PVH blisteris, 1 tablete -
V/DCP/22/0020-08 25 Al/OPA/Al/PVH blisteris, 2 tablete -
V/DCP/22/0020-09 25 Al/OPA/Al/PVH blisteris, 4 tablete -
Alpramil mg V/DCP/22/0021 Alfasan Nederland BV, Nīderlande QP54AB51 cats Vairāk

Medicinal product information

Pharmaceutical form: film-coated tablets
International name (active substance): MILBEMYCINE OXIME, Praziquantel
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 27-May-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (09-Jan-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (09-Jan-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (09-Jan-2026)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/22/0021-01 1 alumīnija/PVC/PE/PVDC blisteris, 1 tablete -
V/DCP/22/0021-02 1 alumīnija/PVC/PE/PVDC blisteris, 2 tablete -
V/DCP/22/0021-03 1 alumīnija/PVC/PE/PVDC blisteris, 4 tablete -
V/DCP/22/0021-04 10 alumīnija/PVC/PE/PVDC blisteris, 1 tablete -
V/DCP/22/0021-05 10 alumīnija/PVC/PE/PVDC blisteris, 2 tablete -
V/DCP/22/0021-06 10 alumīnija/PVC/PE/PVDC blisteris, 4 tablete -
V/DCP/22/0021-07 25 alumīnija/PVC/PE/PVDC blisteris, 1 tablete -
V/DCP/22/0021-08 25 alumīnija/PVC/PE/PVDC blisteris, 2 tablete -
V/DCP/22/0021-09 25 alumīnija/PVC/PE/PVDC blisteris, 4 tablete -
Tulaject 100 mg/ml V/DCP/20/0059 Alivira Animal Health Limited;, Īrija 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 LABORATORIOS KARIZOO, S.A., Spānija
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 (07-Jan-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (07-Jan-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (07-Jan-2026)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/20/0059-01 100 mg/ml 1 Stikla flakons, 50 ml -
V/DCP/20/0059-02 100 mg/ml 1 Stikla flakons, 100 ml -
V/DCP/20/0059-03 100 mg/ml 1 Stikla flakons, 250 ml -
ReproCyc PRRS EU - V/DCP/15/0007 Boehringer Ingelheim Vetmedica GmbH, Vācija QI09AD03 pigs Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and solvent for suspension for injection
International name (active substance): Live attenuated porcine reproductive and respiratory syndrome virus, strain 94881
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Boehringer Ingelheim Pharma GmbH & Co. KG, Vācija
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 (24-Oct-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (24-Oct-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (24-Oct-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/15/0007-01 1 Stikla flakons, 10 deva -
V/DCP/15/0007-02 1 Stikla flakons, 50 deva [PDF] [PDF] [DOCX]
V/DCP/15/0007-03 1 Stikla flakons, 100 deva -
V/DCP/15/0007-04 12 Stikla flakons, 10 deva -
V/DCP/15/0007-05 25 Stikla flakons, 10 deva -
V/DCP/15/0007-06 12 Stikla flakons, 50 deva -
V/DCP/15/0007-07 25 Stikla flakons, 50 deva -
V/DCP/15/0007-08 12 Stikla flakons, 100 deva -
V/DCP/15/0007-09 25 Stikla flakons, 100 deva -
Novasul 500 mg/ml V/NRP/97/0557 VetViva Richter GmbH , Austrija QN02BB02 cattle; pigs; horses; dogs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Metamizole sodium monohydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release VetViva Richter GmbH , Austrija
Date of authorisation/renewal: 20-May-2013
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (01-Jun-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (01-Jun-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (01-Jun-2026)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/97/0557-01 500 mg/ml 1 Stikla flakons ar bromobutila aizbāzni, 100 ml -

3082 records

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