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 5
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
Cartaxx 100 mg V/DCP/25/0075 Alfasan Nederland BV, Nīderlande QM01AE91 dogs Vairāk

Medicinal product information

Pharmaceutical form: chewable tablets
International name (active substance): Carprofen
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 10-Dec-2025
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
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/DCP/25/0075-01 1 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0075-02 2 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0075-03 3 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0075-04 4 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0075-05 5 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0075-06 6 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0075-07 7 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0075-08 8 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0075-09 9 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0075-10 10 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0075-11 12 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0075-12 25 PVH/PE/PVDH-Al blisteris, 10 tablete -
Imaverol 100 mg/ml V/NRP/96/0411 AUDEVARD , Francija QD01AC90 cattle; horses; dogs Vairāk

Medicinal product information

Pharmaceutical form: concentrate for cutaneous emulsion
International name (active substance): Enilconazole
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lusomedicamenta Sociedade Tecnica Farmaceutica, S.A., Portugāle
Date of authorisation/renewal: 14-Aug-2012
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Nov-2025)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (27-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/96/0411-01 100 mg/ml 1 Stikla flakons, 100 ml [PDF] [PDF] [DOCX]
V/NRP/96/0411-02 100 mg/ml 1 Polietilēna flakons, 1000 ml -
Toxicol vet. - V/NRP/03/1611 Zoetis Belgium S.A., Beļģija QI09AB08 pigs Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): E. coli F4ab (K88) antigen,E. coli F4ac (K88 ac) antigen,E. coli F5 (K99) antigen ,E. coli F6 (K987P) antigen,Clostridium perfringens, beta-toxoid (type B and C),Clostridium perfringens, epsilon-toxoid (type D)
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Zoetis Belgium S.A., Beļģija
Date of authorisation/renewal: 08-Dec-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (14-Nov-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (14-Nov-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (14-Nov-2024)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/03/1611-01 1 Flakons, 50 ml -
V/NRP/03/1611-02 1 Flakons, 100 ml -
Poulvac IB Primer - V/MRP/21/0037 Zoetis Belgium S.A., Beļģija QI01AD07 chickens Vairāk

Medicinal product information

Pharmaceutical form: Lyophilisate for suspension for spray, eye drop or drinking water administration
International name (active substance): Live infectious bronchitis virus, strain H120, Live infectious bronchitis virus, strain D274
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Zoetis Manufacturing & Research Spain S.L., Spānija
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 (14-Aug-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (14-Aug-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (14-Aug-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/21/0037-01 10 Stikla flakons, 1000 deva -
V/MRP/21/0037-02 10 Stikla flakons, 2500 deva -
V/MRP/21/0037-03 10 Stikla flakons, 5000 deva -
Poulvac IB QX - V/MRP/13/0019 Zoetis Belgium S.A., Beļģija QI01AD07 chickens Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate for oculonasal suspension
International name (active substance): Live attenuated Avian Infectious BronchitisVirus, Strain L1148
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Zoetis Manufacturing & Research Spain S.L., Spānija
Date of authorisation/renewal: 29-Dec-2015
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 (17-Dec-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/13/0019-01 10 Stikla flakons, 2000 deva -
V/MRP/13/0019-02 10 Stikla flakons, 5000 deva -
V/MRP/13/0019-03 10 Stikla flakons, 10000 deva -
V/MRP/13/0019-04 1 Stikla flakons, 2000 deva -
V/MRP/13/0019-05 1 Stikla flakons, 5000 deva -
V/MRP/13/0019-06 1 Stikla flakons, 10000 deva -
Poulvac NDW - V/MRP/14/0047 Zoetis Belgium S.A., Beļģija QI01AD06 chickens Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate for oculonasal suspension
International name (active substance): Live Newcastle disease virus, strain Ulster 2C
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Zoetis Manufacturing & Research Spain S.L., Spānija
Date of authorisation/renewal: 30-Sep-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (15-Oct-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (15-Oct-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (15-Oct-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/14/0047-01 10 Flakons, 2000 deva -
V/MRP/14/0047-02 10 Flakons, 5000 deva -
Karbaseptas - V/NRP/03/1571 RUVERA, UAB, Lietuva QD02AX cattle; horses; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: ointment
International name (active substance): Methyl salicylate, Camphor
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release Joint-Stock Company "RUVERA", Lietuva;Ruvera UAB, Lietuva
Date of authorisation/renewal: 18-Aug-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (19-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (19-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (19-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/03/1571-01 1 Polipropilēna trauciņš, 100 g -
V/NRP/03/1571-04 1 Polipropilēna trauciņš, 250 g -
V/NRP/03/1571-06 1 Polipropilēna spainis, 1 kg -
V/NRP/03/1571-07 1 ABPE spainis/PE vāciņš, 10 kg -
V/NRP/03/1571-08 1 PP spainis/PP vāciņš, 18 kg -
V/NRP/03/1571-10 1 PP spainis/PP vāciņš, 10 kg -
Rispoval IBR-Marker Inactivatum - V/MRP/08/1573 Zoetis Belgium S.A., Beļģija QI02AA03 cattle Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Bovine Herpes virus type 1, strain Difivac (IBR-Marker Virus, gE negative)
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Zoetis Belgium S.A., Beļģija
Date of authorisation/renewal: 03-Dec-2009
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
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/MRP/08/1573-02 1 Stikla flakons, 10 deva -
V/MRP/08/1573-03 1 Stikla flakons, 50 deva -
Thiamavance 10 mg/ml V/DCP/25/0078 VIRBAC, Francija QH03BB02 cats Vairāk

Medicinal product information

Pharmaceutical form: Oral solution
International name (active substance): Thiamazol
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 18-Dec-2025
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (18-Dec-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (18-Dec-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (18-Dec-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/25/0078-01 1 Stikla pudele (šļirce graduēta pa 0,5 mg iedaļām), 30 ml -
V/DCP/25/0078-02 1 Stikla pudele (šļirce graduēta pa 1,25 mg iedaļām), 30 ml -
Supprestral injectable 50 mg/ml V/NRP/03/1579 Vetoquinol S.A., Francija QG03AC06 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Medroxyprogesterone acetate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Vetoquinol S.A., Francija
Date of authorisation/renewal: 22-Sep-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [DOC] 267-220908LI (22-Sep-2008)
Labelling text: [DOC] 220908M (22-Sep-2008)
Summary of product characteristics: [DOC] 267-220908ZA (22-Sep-2008)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/03/1579-01 50 mg/ml 1 Flakons, 5 ml -
Covexin 10 - V/MRP/10/0020 Zoetis Belgium S.A., Beļģija QI04AB01;QI02AB01 cattle; sheep Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Clostridium perfringens, epsilon-toxoid (type D), Clostridium perfringens, beta-toxoid (type B and C), Toxoid Clostridium novyi, Clostridium tetani toxoid, C. perfringens type A toxoid, C. chauvoei whole culture, C. septicum toxoid, C. sordellii toxoid, C. haemolyticum toxoid
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Pfizer Animal Health S.A., Beļģija
Date of authorisation/renewal: 31-Mar-2015
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (23-Nov-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (23-Nov-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (23-Nov-2023)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/10/0020-02 1 Polietilēna pudele, 50 ml -
V/MRP/10/0020-03 1 Polietilēna pudele, 100 ml -
Rispoval 3 BRSV Pi3 BVD - V/MRP/05/1643 Zoetis Belgium S.A., Beļģija QI02AH cattle Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and suspension for suspension for injection
International name (active substance): Bovine Viral Diarrhoea Virus (BVD), strain 6309, killed,Bovine Parainfluenza 3 virus (Pi3) RLB 103 attennuated,Inactivated Bovine Viral Diarrhoea virus, cytopathic strain 5960,Bovine respiratory syncytial virus
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Zoetis Animal Health SA, Beļģija
Date of authorisation/renewal: 31-Mar-2010
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
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/MRP/05/1643-01 1 Stikla flakons, 5 deva -
V/MRP/05/1643-02 1 Stikla flakons, 25 deva -
Kolibin RC NEO - V/NRP/18/0033 Bioveta, a.s., Čehija QI02AL01 cattle Vairāk

Medicinal product information

Pharmaceutical form: emulsion for injection
International name (active substance): Inactivated E.coli bacteria,Inactivated bovine coronavirus strain C-197,Inactivated Bovine rotavirus, strain TM-91
Distribution category: To be supplied only on veterinary prescription
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: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Feb-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Feb-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (16-Feb-2026)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/18/0033-01 2 Stikla flakons, 1 deva -
V/NRP/18/0033-02 10 Stikla flakons, 1 deva -
V/NRP/18/0033-03 20 Stikla flakons, 1 deva -
V/NRP/18/0033-04 1 Stikla flakons, 2 deva -
V/NRP/18/0033-05 5 Stikla flakons, 2 deva -
V/NRP/18/0033-06 10 Stikla flakons, 2 deva -
V/NRP/18/0033-07 1 Stikla flakons, 5 deva -
V/NRP/18/0033-08 1 Plastikāta flakons, 5 deva -
V/NRP/18/0033-09 5 Stikla flakons, 5 deva -
V/NRP/18/0033-10 5 Plastikāta flakons, 5 deva -
V/NRP/18/0033-11 10 Stikla flakons, 5 deva -
V/NRP/18/0033-12 10 Plastikāta flakons, 5 deva -
V/NRP/18/0033-13 1 Stikla flakons, 10 deva -
V/NRP/18/0033-14 5 Stikla flakons, 10 deva -
V/NRP/18/0033-15 10 Stikla flakons, 10 deva -
V/NRP/18/0033-16 1 Stikla flakons, 25 deva -
V/NRP/18/0033-17 1 Plastikāta flakons, 25 deva -
V/NRP/18/0033-18 12 Stikla flakons, 25 deva -
V/NRP/18/0033-19 12 Plastikāta flakons, 25 deva -
V/NRP/18/0033-20 24 Stikla flakons, 25 deva -
V/NRP/18/0033-21 24 Plastikāta flakons, 25 deva -
V/NRP/18/0033-22 1 Stikla flakons, 50 deva -
V/NRP/18/0033-23 1 Plastikāta flakons, 50 deva -
V/NRP/18/0033-24 12 Stikla flakons, 50 deva -
V/NRP/18/0033-25 12 Plastikāta flakons, 50 deva -
V/NRP/18/0033-26 20 Stikla flakons, 50 deva -
V/NRP/18/0033-27 20 Plastikāta flakons, 50 deva -
V/NRP/18/0033-28 1 Plastikāta flakons, 125 deva -
V/NRP/18/0033-29 12 Plastikāta flakons, 125 deva -
V/NRP/18/0033-30 20 Plastikāta flakons, 125 deva -
PestiGon Combo 402 mg / 361,8 mg - V/DCP/17/0017 Norbrook Laboratories (Ireland) Limited, Īrija QP53AX65 very large dogs 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 Norbrook Laboratories Limited, Lielbritānija;Norbrook Manufacturing Limited, Īrija
Date of authorisation/renewal: 29-Mar-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 29032022LI (29-Mar-2022)
Labelling text: [DOCX] 29032022M (29-Mar-2022)
Summary of product characteristics: [DOCX] 29032022ZA (29-Mar-2022)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/17/0017-01 1 Pipete, 1 deva -
V/DCP/17/0017-02 2 Pipete, 1 deva -
V/DCP/17/0017-03 3 Pipete, 1 deva -
V/DCP/17/0017-04 4 Pipete, 1 deva -
V/DCP/17/0017-05 6 Pipete, 1 deva -
V/DCP/17/0017-06 8 Pipete, 1 deva -
V/DCP/17/0017-07 12 Pipete, 1 deva -
V/DCP/17/0017-08 24 Pipete, 1 deva -
V/DCP/17/0017-09 30 Pipete, 1 deva -
V/DCP/17/0017-10 60 Pipete, 1 deva -
V/DCP/17/0017-11 90 Pipete, 1 deva -
V/DCP/17/0017-12 120 Pipete, 1 deva -
V/DCP/17/0017-13 150 Pipete, 1 deva -
Noroclox DC 500 mg V/NRP/96/0443 Norbrook Laboratories (Ireland) Limited, Īrija QJ51CF02 cows 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 Norbrook Laboratories Limited, Lielbritānija;Norbrook Manufacturing Limited, Īrija
Date of authorisation/renewal: 16-Apr-2008
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/96/0443-01 500 mg 24 Injektors, 1 deva -
V/NRP/96/0443-02 500 mg 120 Injektors, 1 deva -
BioRabbit RHDV 1,2 - V/DCP/23/0007 Bioveta, a.s., Čehija QI08AA01 rabbits Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Rabbit haemorrhagic disease virus 2, Inactivated, Rabbit haemorrhagic disease virus, Inactivated
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bioveta a.s., Čehija
Date of authorisation/renewal: 28-Mar-2023
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (22-Jun-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (22-Jun-2023)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (22-Jun-2023)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/23/0007-01 10 Stikla flakons (plastmasas kastē), 1 deva -
V/DCP/23/0007-02 10 Stikla flakons (plastmasas kastē), 10 deva -
V/DCP/23/0007-03 10 Stikla flakons (plastmasas kastē), 20 deva -
V/DCP/23/0007-04 1 ABPE flakons (kartona kastē), 10 deva -
V/DCP/23/0007-05 1 ABPE flakons (kartona kastē), 20 deva -
V/DCP/23/0007-06 1 Stikla flakons (kartona kastē), 10 deva -
V/DCP/23/0007-07 1 Stikla flakons (kartona kastē), 20 deva -
V/DCP/23/0007-08 10 ABPE flakons (plastmasas kastē), 10 deva -
V/DCP/23/0007-09 10 ABPE flakons (plastmasas kastē), 20 deva -
Seton 2% 20 mg/ml V/NRP/02/1422 Laboratorios Calier, S.A., Spānija QN05CM92 cattle; horses; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Xylazine hydrochloride
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release Laboratorios Calier, S.A., Spānija
Date of authorisation/renewal: 21-May-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 211116LI (02-Dec-2016)
Labelling text: [PDF] 211116M (02-Dec-2016)
Summary of product characteristics: [PDF] 211116ZA (02-Dec-2016)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/02/1422-01 1 Flakons, 25 ml -
V/NRP/02/1422-02 1 Flakons, 10 ml -
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 -

3082 records

© Food and veterinary service · 2026 Cookies policy