Veterinary medicinal product register

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Data selected by 2
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
Cardisan 10 mg V/DCP/22/0053 Alfasan Nederland BV, Nīderlande QC01CE90 dogs Vairāk

Medicinal product information

Pharmaceutical form: chewable tablets
International name (active substance): Pimobendan
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Alfasan Nederland BV, Nīderlande;Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 19-Dec-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (19-Dec-2022)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (19-Dec-2022)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (19-Dec-2022)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/22/0053-01 10 mg 3 Al/OPA/Al/PVH blisteris, 10 tablete -
V/DCP/22/0053-02 10 mg 6 Al/OPA/Al/PVH blisteris, 10 tablete -
V/DCP/22/0053-03 10 mg 9 Al/OPA/Al/PVH blisteris, 10 tablete -
V/DCP/22/0053-04 10 mg 10 Al/OPA/Al/PVH blisteris, 10 tablete -
V/DCP/22/0053-05 10 mg 12 Al/OPA/Al/PVH blisteris, 10 tablete -
Cardisan 15 mg V/DCP/22/0054 Alfasan Nederland BV, Nīderlande QC01CE90 dogs Vairāk

Medicinal product information

Pharmaceutical form: chewable tablets
International name (active substance): Pimobendan
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Alfasan Nederland BV, Nīderlande;Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 19-Dec-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (19-Dec-2022)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (19-Dec-2022)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (19-Dec-2022)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/22/0054-01 15 mg 6 Al/OPA/Al/PVH blisteris, 5 tablete -
V/DCP/22/0054-02 15 mg 12 Al/OPA/Al/PVH blisteris, 5 tablete -
V/DCP/22/0054-03 15 mg 18 Al/OPA/Al/PVH blisteris, 5 tablete -
V/DCP/22/0054-04 15 mg 20 Al/OPA/Al/PVH blisteris, 5 tablete -
V/DCP/22/0054-05 15 mg 24 Al/OPA/Al/PVH blisteris, 5 tablete -
Ceftiosan 50 mg/ml V/DCP/12/0003 Alfasan Nederland BV, Nīderlande QJ01DD90 cattle; pigs Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Ceftiofur (as ceftiofur hydrochloride)
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Alfasan Nederland BV, Nīderlande
Date of authorisation/renewal: 07-Mar-2016
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] 200317LI (22-Mar-2017)
Labelling text: [PDF] 200317M (22-Mar-2017)
Summary of product characteristics: [PDF] 200317ZA (22-Mar-2017)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/12/0003-01 50 mg/ml 1 Stikla flakons, 100 ml -
V/DCP/12/0003-02 50 mg/ml 12 Stikla flakons, 100 ml -
V/DCP/12/0003-03 50 mg/ml 1 Stikla flakons, 250 ml -
V/DCP/12/0003-04 50 mg/ml 6 Stikla flakons, 250 ml -
V/DCP/12/0003-05 50 mg/ml 1 Stikla flakons, 50 ml -
V/DCP/12/0003-06 50 mg/ml 15 Stikla flakons, 50 ml -
Nobivac Respira Bb - V/DCP/20/0055 Intervet International B.V., Nīderlande QI07AB03 dogs Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection in pre-filled syringes
International name (active substance): Bordetella bronchiseptica fimbriae
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: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Feb-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Feb-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (27-Feb-2023)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/20/0055-01 5 Stikla pilnšļirce, 1 deva -
V/DCP/20/0055-02 10 Stikla pilnšļirce, 1 deva -
Nobivac Respira Bb - V/DCP/20/0056 Intervet International B.V., Nīderlande QI07AB03 dogs Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Bordetella bronchiseptica fimbriae
Distribution category: To be used only by veterinary surgeon
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: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Feb-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Feb-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (27-Feb-2023)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/20/0056-01 1 Polietilēna flakons, 10 deva -
Exitel Plus - V/MRP/09/0028 Chanelle Pharmaceuticals Manufacturing Ltd., Īrija QP52AA51 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Febantel,Praziquantel,Pyrantel embonate
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release Chanelle Pharmaceuticals Manufacturing Ltd., Īrija
Date of authorisation/renewal: 08-Apr-2014
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (30-May-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (30-May-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (23-Jul-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/09/0028-01 2 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-02 4 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-03 6 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-04 8 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-05 10 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-06 12 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-07 14 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-08 16 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-09 18 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-10 20 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-11 24 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-12 28 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-13 30 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-14 32 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-15 36 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-16 40 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-17 42 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-18 44 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-19 48 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-20 50 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-21 52 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-22 56 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-23 60 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-24 70 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-25 80 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-26 84 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-27 90 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-28 98 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-29 100 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-30 104 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-31 106 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-32 120 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-33 140 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-34 150 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-35 180 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-36 200 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-37 204 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-38 206 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-39 250 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-40 280 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-41 300 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-42 500 Alumīnija blisteris, 1 tablete -
V/MRP/09/0028-43 1000 Alumīnija blisteris, 1 tablete -
Cepedol Vet 80 mg V/DCP/24/0020 CP-Pharma Handelsgesellschaft GmbH, Vācija QN02AX02 dogs Vairāk

Medicinal product information

Pharmaceutical form: chewable tablets
International name (active substance): Tramadol hydrochloride
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release CP-Pharma Handelsgesellschaft GmbH, Vācija
Date of authorisation/renewal: 20-Feb-2024
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Feb-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Feb-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (20-Feb-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/24/0020-01 1 AL/PVC-AL-PA blisteris, 10 tablete -
V/DCP/24/0020-02 3 AL/PVC-AL-PA blisteris, 10 tablete -
V/DCP/24/0020-03 5 AL/PVC-AL-PA blisteris, 10 tablete -
V/DCP/24/0020-04 10 AL/PVC-AL-PA blisteris, 10 tablete -
Cepedol Vet 120 mg V/DCP/24/0021 CP-Pharma Handelsgesellschaft GmbH, Vācija QN02AX02 dogs Vairāk

Medicinal product information

Pharmaceutical form: chewable tablets
International name (active substance): Tramadol hydrochloride
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release CP-Pharma Handelsgesellschaft GmbH, Vācija
Date of authorisation/renewal: 20-Feb-2024
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Feb-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Feb-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (20-Feb-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/24/0021-01 1 AL/PVC-AL-PA blisteris, 10 tablete -
V/DCP/24/0021-02 3 AL/PVC-AL-PA blisteris, 10 tablete -
V/DCP/24/0021-03 5 AL/PVC-AL-PA blisteris, 10 tablete -
V/DCP/24/0021-04 10 AL/PVC-AL-PA blisteris, 10 tablete -
Deltanil 10 mg/ml V/DCP/13/0037 VIRBAC, Francija QP53AC11 cattle; sheep Vairāk

Medicinal product information

Pharmaceutical form: Pour-on solution
International name (active substance): Deltamethrin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release VIRBAC, Francija
Date of authorisation/renewal: 01-Apr-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (23-May-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (23-May-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (23-May-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/13/0037-01 10 mg/ml 1 Polietilēna pudele, 500 ml -
V/DCP/13/0037-02 10 mg/ml 1 Polietilēna pudele, 1 l -
V/DCP/13/0037-03 10 mg/ml 1 Polietilēna pudele, 2,5 l -
V/DCP/13/0037-04 10 mg/ml 1 Maiss, 4,5 l -
V/DCP/13/0037-05 10 mg/ml 1 Maiss, 2,5 l -
Tsefalen 1000 mg V/DCP/12/0058 NEXTMUNE ITALY S.R.L., Itālija QJ01DB01 dogs Vairāk

Medicinal product information

Pharmaceutical form: film-coated tablets
International name (active substance): Cefalexin monohydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Facta Farmaceutici Spa , Itālija
Date of authorisation/renewal: 31-Jul-2017
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (25-Feb-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (25-Feb-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (25-Feb-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/12/0058-01 1000 mg 1 PVH/Al blisteris, 8 tablete -
V/DCP/12/0058-02 1000 mg 13 PVH/Al blisteris, 8 tablete -
V/DCP/12/0058-03 1000 mg 4 PVH/Al blisteris, 8 tablete -
Calcibel Forte - V/DCP/21/0049 Bela-pharm GmbH&Co.KG, Vācija QA12AX cattle; pigs; sheep; goats; horses Vairāk

Medicinal product information

Pharmaceutical form: solution for infusion
International name (active substance): Calcium gluconate, Magnesium chloride hexahydrate, Boric Acid
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: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (04-Jun-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (04-Jun-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (04-Jun-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/21/0049-01 1 Polipropilēna pudele, 500 ml -
V/DCP/21/0049-02 12 Polipropilēna pudele, 500 ml -
Cepralock 2.6 g V/DCP/21/0013 Intervet International B.V., Nīderlande QG52X cattle Vairāk

Medicinal product information

Pharmaceutical form: intramammary suspension
International name (active substance): Bismuth subnitrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Intervet International GmbH, Vācija
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 (14-Jan-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (14-Jan-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (14-Jan-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/21/0013-01 2,6 g 24 Injektors, 4 g -
V/DCP/21/0013-02 2,6 g 144 Injektors, 4 g -
Amflee 134 mg V/DCP/13/0046 KRKA, d.d., Novo mesto, Slovēnija QP53AX15 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 KRKA, d.d., Novo mesto, Slovēnija
Date of authorisation/renewal: 30-Jan-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (20-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/13/0046-01 134 mg 1 Polipropilēna pipete, 1 deva -
V/DCP/13/0046-02 134 mg 3 Polipropilēna pipete, 1 deva -
V/DCP/13/0046-03 134 mg 6 Polipropilēna pipete, 1 deva -
V/DCP/13/0046-04 134 mg 10 Polipropilēna pipete, 1 deva -
V/DCP/13/0046-05 134 mg 20 Polipropilēna pipete, 1 deva -
Amflee 268 mg V/DCP/13/0047 KRKA, d.d., Novo mesto, Slovēnija QP53AX15 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 KRKA, d.d., Novo mesto, Slovēnija
Date of authorisation/renewal: 30-Jan-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (20-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/13/0047-01 268 mg 1 Polipropilēna pipete, 1 deva -
V/DCP/13/0047-02 268 mg 3 Polipropilēna pipete, 1 deva -
V/DCP/13/0047-03 268 mg 6 Polipropilēna pipete, 1 deva -
V/DCP/13/0047-04 268 mg 10 Polipropilēna pipete, 1 deva -
V/DCP/13/0047-05 268 mg 20 Polipropilēna pipete, 1 deva -
Cyclavance 100 mg/ml V/DCP/14/0008 VIRBAC, Francija QL04AD01 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for oral use
International name (active substance): Ciclosporin
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: 31-Oct-2018
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (18-Dec-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (18-Dec-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (18-Dec-2023)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/14/0008-01 100 mg/ml 1 Stikla flakons ar ABPE skrūvējamo vāciņu, 5 ml -
V/DCP/14/0008-02 100 mg/ml 1 Stikla flakons ar ABPE skrūvējamo vāciņu, 15 ml -
V/DCP/14/0008-03 100 mg/ml 1 Stikla flakons ar ABPE skrūvējamo vāciņu, 30 ml -
V/DCP/14/0008-04 100 mg/ml 1 Stikla flakons ar ABPE skrūvējamo vāciņu, 60 ml -
V/DCP/14/0008-05 100 mg/ml 1 Stikla flakons ar bromobutila aizbāzni, 50 ml -
V/DCP/14/0008-06 100 mg/ml 1 Stikla flakons ar bromobutila aizbāzni, 5 ml -
V/DCP/14/0008-07 100 mg/ml 1 Stikla flakons ar bromobutila aizbāzni, 15 ml -
V/DCP/14/0008-08 100 mg/ml 1 Stikla flakons ar bromobutila aizbāzni, 30 ml -
Marbonor 100 mg/ml V/DCP/12/0059 Norbrook Laboratories (Ireland) Limited, Īrija 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 Norbrook Laboratories Limited, Lielbritānija;Norbrook Manufacturing Limited, Īrija
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 (25-Apr-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (25-Apr-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (25-Apr-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/12/0059-09 100 mg/ml 1 Stikla flakons, 50 ml -
V/DCP/12/0059-10 100 mg/ml 1 Stikla flakons, 100 ml -
V/DCP/12/0059-11 100 mg/ml 1 Stikla flakons, 250 ml -
V/DCP/12/0059-12 100 mg/ml 1 Stikla flakons, 500 ml -
V/DCP/12/0059-13 100 mg/ml 1 Plastikāta flakons, 60 ml -
V/DCP/12/0059-14 100 mg/ml 1 Plastikāta flakons, 100 ml -
V/DCP/12/0059-15 100 mg/ml 1 Plastikāta flakons, 250 ml -
V/DCP/12/0059-16 100 mg/ml 1 Plastikāta flakons, 500 ml -
V/DCP/12/0059-17 100 mg/ml 1 Stikla flakons, 20 ml -
Tulieve 100 mg/ml V/DCP/20/0023 Norbrook Laboratories (Ireland) 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 Norbrook Laboratories Limited, Lielbritānija;Norbrook Laboratories (Ireland) Limited, Īrija
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 (13-Jun-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (13-Jun-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (13-Jun-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/20/0023-01 100 mg 1 Stikla flakons, 50 ml -
V/DCP/20/0023-02 100 mg 1 Stikla flakons, 100 ml -
V/DCP/20/0023-03 100 mg 1 Stikla flakons, 250 ml -
V/DCP/20/0023-04 100 mg 1 Stikla flakons, 500 ml -
V/DCP/20/0023-05 100 mg 1 Plastikāta flakons, 50 ml -
V/DCP/20/0023-06 100 mg 1 Plastikāta flakons, 100 ml -
V/DCP/20/0023-07 100 mg 1 Plastikāta flakons, 250 ml -
V/DCP/20/0023-08 100 mg 1 Plastikāta flakons, 500 ml -
V/DCP/20/0023-09 100 mg 1 Plastikāta flakons, 1000 ml -
INTRAMAR PROPEN 3.0 g V/DCP/26/0020 Bioveta a.s., Čehija QJ51CE09 cattle (lactating cows) Vairāk

Medicinal product information

Pharmaceutical form: intramammary suspension
International name (active substance): Benzylpenicillin procaine monohydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bioveta, a.s., Čehija
Date of authorisation/renewal: 14-Apr-2026
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (14-Apr-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (14-Apr-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (14-Apr-2026)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/26/0020-01 24 Injektors (un dezinfekcijas salvetes), 10 ml -
Prid Delta 1.55 g V/MRP/13/0035 Ceva Sante Animale', Francija QG03DA04 cattle Vairāk

Medicinal product information

Pharmaceutical form: vaginal delivery system
International name (active substance): Progesterone
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Ceva Sante Animale, Francija
Date of authorisation/renewal: 29-May-2015
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Apr-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Apr-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (10-Apr-2026)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/13/0035-01 1,55 g 10 Maisiņš (kartona kastē), 1 deva -
V/MRP/13/0035-02 1,55 g 25 Maisiņš (kartona kastē), 1 deva -
V/MRP/13/0035-03 1,55 g 50 Maisiņš (kartona kastē), 1 deva -
V/MRP/13/0035-04 1,55 g 50 Maisiņš (polietilēna kastē), 1 deva -
V/MRP/13/0035-05 1,55 g 10 Polietilēna maisiņš, 1 deva -
V/MRP/13/0035-06 1,55 g 100 Maisiņš (kartona kastē), 1 deva -
V/MRP/13/0035-07 1,55 g 25 Maisiņš (kartona kastē ar aplikatoru), 1 deva -
V/MRP/13/0035-08 1,55 g 50 Maisiņš (kartona kastē ar aplikatoru), 1 deva -
V/MRP/13/0035-09 1,55 g 50 Maisiņš (polietilēna kastē ar aplikatoru), 1 deva -
Gabbrovet 140 mg/ml V/DCP/18/0008 Ceva Sante Animale', Francija QA07AA06 cattle; pigs Vairāk

Medicinal product information

Pharmaceutical form: solution for use in drinking water, milk or milk replacer
International name (active substance): Paromomycin sulfate
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 (07-Apr-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (07-Apr-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (07-Apr-2026)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/18/0008-01 1 ABPE pudele kastē, 125 ml -
V/DCP/18/0008-02 1 ABPE pudele kastē, 250 ml -
V/DCP/18/0008-03 1 ABPE pudele kastē, 500 ml -
V/DCP/18/0008-04 1 ABPE pudele kastē, 1000 ml -
V/DCP/18/0008-05 1 ABPE pudele, 125 ml -
V/DCP/18/0008-06 1 ABPE pudele, 250 ml -
V/DCP/18/0008-07 1 ABPE pudele, 500 ml -
V/DCP/18/0008-08 1 ABPE pudele, 1000 ml -

3081 record

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