Veterinary medicinal product register

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Data selected by 690
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
Myodine vet 25 mg/ml V/DCP/17/0025 Le Vet Beheer B.V., Nīderlande QA14AB01 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Nandrolone laurate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Produlab Pharma b.v., Nīderlande
Date of authorisation/renewal: 26-May-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 26052022LI (26-May-2022)
Labelling text: [DOCX] 26052022M (26-May-2022)
Summary of product characteristics: [DOCX] 26052022ZA (26-May-2022)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/17/0025-01 25 mg/ml 1 Stikla flakons, 5 ml -
V/DCP/17/0025-02 25 mg/ml 6 Stikla flakons, 5 ml -
V/DCP/17/0025-03 25 mg/ml 10 Stikla flakons, 5 ml -
V/DCP/17/0025-04 25 mg/ml 1 Stikla flakons, 10 ml -
V/DCP/17/0025-05 25 mg/ml 6 Stikla flakons, 10 ml -
V/DCP/17/0025-06 25 mg/ml 10 Stikla flakons, 10 ml -
V/DCP/17/0025-07 25 mg/ml 1 Stikla flakons, 20 ml -
V/DCP/17/0025-08 25 mg/ml 6 Stikla flakons, 20 ml -
V/DCP/17/0025-09 25 mg/ml 10 Stikla flakons, 20 ml -
Pimocard 3.5 mg/ml V/DCP/19/0068 Dechra Regulatory B.V., Nīderlande QC01CE90 dogs Vairāk

Medicinal product information

Pharmaceutical form: solution for oral use
International name (active substance): Pimobendan
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release GENERA Inc., Horvātija
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 240120LI (24-Jan-2020)
Labelling text: [DOCX] 260722M (26-Jul-2022)
Summary of product characteristics: [DOCX] 260722ZA (26-Jul-2022)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/19/0068-01 3,5 mg/ml 1 PET pudele, 42 ml -
V/DCP/19/0068-02 3,5 mg/ml 1 PET pudele, 168 ml -
Atipam 5 mg/ml V/DCP/08/1599 Eurovet Animal Health B.V., Nīderlande QV03AB90 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Atipamezole hydrochloride
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release Eurovet Animal Health B.V., Nīderlande
Date of authorisation/renewal: 20-May-2013
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (04-Dec-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (04-Dec-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (04-Dec-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/08/1599-01 5 mg/ml 1 Stikla flakons, 5 ml -
V/DCP/08/1599-02 5 mg/ml 1 Stikla flakons, 10 ml -
V/DCP/08/1599-03 5 mg/ml 1 Stikla flakons, 20 ml -
Laxatract 667 mg/ml V/DCP/19/0010 Dechra Regulatory B.V., Nīderlande QA06AD11 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: syrup
International name (active substance): Lactulose
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Feramed B.V., Nīderlande
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] 29032019_LI (03-Apr-2019)
Labelling text: [PDF] 29032019_M (03-Apr-2019)
Summary of product characteristics: [PDF] 29032019_ZA (03-Apr-2019)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/19/0010-01 667 mg/ml 1 ABPE pudele, 50 ml -
V/DCP/19/0010-02 667 mg/ml 1 ABPE pudele, 125 ml -
V/DCP/19/0010-03 667 mg/ml 1 ABPE pudele, 325 ml -
Rycarfa 50 mg/ml V/DCP/10/0026 KRKA, d.d., Novo mesto, Slovēnija 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 KRKA, d.d., Novo mesto, Slovēnija
Date of authorisation/renewal: 29-Sep-2015
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (12-Dec-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (12-Dec-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (12-Dec-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/10/0026-01 50 mg/ml 1 Stikla flakons, 20 ml -
RABADROP - V/DCP/19/0059 Bioveta, a.s., Čehija QI07BD raccoon dogs; foxes Vairāk

Medicinal product information

Pharmaceutical form: suspension for oral use
International name (active substance): Attenuated rabies virus, strain SAD Clone
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: DCP
Package leaflet: [DOCX] 24032021LI (24-Mar-2021)
Labelling text: [PDF] 04102019M (04-Oct-2019)
Summary of product characteristics: [DOCX] 23032021ZA (24-Mar-2021)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/19/0059-01 1 PVH/Al blisteris, 20 deva -
V/DCP/19/0059-02 30 PVH/Al blisteris, 20 deva -
V/DCP/19/0059-03 1 PVH/Al blisteris, 30 deva -
V/DCP/19/0059-04 1 PVH/Al blisteris, 700 deva -
V/DCP/19/0059-05 2 PVH/Al blisteris, 350 deva [PDF]
Alfafer 10% 100 mg/ml V/NRP/97/0600 Alfasan International B.V., Nīderlande QB03AC calves; piglets Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Iron
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Alfasan International B.V., Nīderlande
Date of authorisation/renewal: 22-Sep-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 19062018LI (19-Jun-2018)
Labelling text: [PDF] 19062018M (19-Jun-2018)
Summary of product characteristics: [PDF] 19062018ZA (19-Jun-2018)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/97/0600-01 100 mg/ml 1 Stikla (tumša) flakons, 50 ml -
V/NRP/97/0600-03 100 mg/ml 1 Stikla (tumša) flakons, 100 ml -
Amoxyn 100% - V/NRP/07/1708 LAVET Pharmaceuticals Ltd., Ungārija QJ01CA04 pigs; turkeys; chickens Vairāk

Medicinal product information

Pharmaceutical form: powder for oral solution
International name (active substance): Amoxicillin trihydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release LAVET Pharmaceuticals Ltd., Ungārija
Date of authorisation/renewal: 30-May-2013
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [DOCX] 03012022LI (04-Jan-2022)
Labelling text: [DOCX] 03012022M (04-Jan-2022)
Summary of product characteristics: [DOCX] 03012022ZA (04-Jan-2022)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/07/1708-01 1000 mg/g 1 Polietilēna konteiners, 100 g -
V/NRP/07/1708-02 1000 mg/g 1 Polietilēna konteiners, 1 kg -
V/NRP/07/1708-03 1000 mg/g 1 Polietilēna konteiners, 5 kg -
SET-VAC - V/NRP/17/0022 Optim Vet, Latvija QI01AB01 chickens Vairāk

Medicinal product information

Pharmaceutical form: emulsion for injection
International name (active substance): Inactivated Salmonella Typhimurium, strain DT104, Inactivated Salmonella Enteritidis PT4
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release FATRO S.p.A., Itālija
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [DOCX] 27012022LI (28-Jan-2022)
Labelling text: [DOCX] 27012022M (28-Jan-2022)
Summary of product characteristics: [DOCX] 27012022ZA (28-Jan-2022)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/17/0022-01 10 Stikla flakons, 500 deva -
V/NRP/17/0022-02 10 Stikla flakons, 1000 deva -
V/NRP/17/0022-03 10 Polipropilēna flakons, 500 deva -
V/NRP/17/0022-04 10 Polipropilēna flakons, 1000 deva -
Fipron 402 mg V/MRP/16/0024 Bioveta, a.s., Čehija QP53AX15 very large 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/16/0024-01 402 mg/deva 1 Polietilēna tūbiņa, 1 deva -
V/MRP/16/0024-02 402 mg/deva 3 Polietilēna tūbiņa, 1 deva -
V/MRP/16/0024-03 402 mg/deva 25 Polietilēna tūbiņa, 1 deva -
Dinalgen 150 mg/ml V/MRP/11/0052 ECUPHAR VETERINARIA S.L.U, Spānija QM01AE03 cattle; pigs; horses Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Ketoprofen
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: 27-Apr-2015
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
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/MRP/11/0052-01 150 mg/ml 1 Stikla flakons, 100 ml -
V/MRP/11/0052-02 150 mg/ml 5 Stikla flakons, 100 ml -
V/MRP/11/0052-03 150 mg/ml 10 Stikla flakons, 100 ml -
V/MRP/11/0052-04 150 mg/ml 1 Stikla flakons, 250 ml -
V/MRP/11/0052-05 150 mg/ml 5 Stikla flakons, 250 ml -
Milprazon CHEWABLE 16 mg/40 mg - V/MRP/19/0012 KRKA, d.d., Novo mesto, Slovēnija QP54AB51 cats weighing at least 2 kg Vairāk

Medicinal product information

Pharmaceutical form: film-coated tablets
International name (active substance): Milbemycin oxime, Praziquantel
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release KRKA d.d. Novo Mesto, Slovēnija
Date of authorisation/renewal: 02-May-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Sep-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Sep-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (17-Sep-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/19/0012-01 16/40 mg 1 Al/OPA/Al/PVH blisteris, 2 tablete -
V/MRP/19/0012-02 16/40 mg 1 Al/OPA/Al/PVH blisteris, 4 tablete -
V/MRP/19/0012-03 16/40 mg 12 Al/OPA/Al/PVH blisteris, 4 tablete -
Clavaseptin 500 mg - V/MRP/11/0036 Vetoquinol S.A., Francija QJ01CR02 dogs Vairāk

Medicinal product information

Pharmaceutical form: palatable tablets
International name (active substance): Amoxicillin trihydrate,Clavulanic acid
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Vetoquinol S.A., Francija
Date of authorisation/renewal: 31-Oct-2014
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Dec-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Dec-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (06-Dec-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/11/0036-01 1 Alumīnija blisteris, 10 tablete -
V/MRP/11/0036-02 2 Alumīnija blisteris, 10 tablete -
V/MRP/11/0036-03 5 Alumīnija blisteris, 10 tablete -
V/MRP/11/0036-04 10 Alumīnija blisteris, 10 tablete -
V/MRP/11/0036-05 12 Alumīnija blisteris, 10 tablete -
V/MRP/11/0036-06 15 Alumīnija blisteris, 10 tablete -
V/MRP/11/0036-07 20 Alumīnija blisteris, 10 tablete -
V/MRP/11/0036-08 25 Alumīnija blisteris, 10 tablete -
V/MRP/11/0036-09 30 Alumīnija blisteris, 10 tablete -
V/MRP/11/0036-10 40 Alumīnija blisteris, 10 tablete -
V/MRP/11/0036-11 50 Alumīnija blisteris, 10 tablete -
V/MRP/11/0036-12 60 Alumīnija blisteris, 10 tablete -
V/MRP/11/0036-13 75 Alumīnija blisteris, 10 tablete -
V/MRP/11/0036-14 100 Alumīnija blisteris, 10 tablete -
Clavaseptin 250 mg - V/MRP/11/0037 Vetoquinol S.A., Francija QJ01CR02 dogs Vairāk

Medicinal product information

Pharmaceutical form: palatable tablets
International name (active substance): Amoxicillin trihydrate,Clavulanic acid
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Vetoquinol S.A., Francija
Date of authorisation/renewal: 31-Oct-2014
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Dec-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Dec-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (06-Dec-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/11/0037-01 1 Alumīnija blisteris, 10 tablete -
V/MRP/11/0037-02 2 Alumīnija blisteris, 10 tablete -
V/MRP/11/0037-03 5 Alumīnija blisteris, 10 tablete -
V/MRP/11/0037-04 10 Alumīnija blisteris, 10 tablete -
V/MRP/11/0037-05 12 Alumīnija blisteris, 10 tablete -
V/MRP/11/0037-06 15 Alumīnija blisteris, 10 tablete -
V/MRP/11/0037-07 20 Alumīnija blisteris, 10 tablete -
V/MRP/11/0037-08 25 Alumīnija blisteris, 10 tablete -
V/MRP/11/0037-09 30 Alumīnija blisteris, 10 tablete -
V/MRP/11/0037-10 40 Alumīnija blisteris, 10 tablete -
V/MRP/11/0037-11 50 Alumīnija blisteris, 10 tablete -
V/MRP/11/0037-12 60 Alumīnija blisteris, 10 tablete -
V/MRP/11/0037-13 75 Alumīnija blisteris, 10 tablete -
V/MRP/11/0037-14 100 Alumīnija blisteris, 10 tablete -
Porcilis Glässer - V/MRP/05/1623 Intervet International B.V., Nīderlande QI09AB07 pigs Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Inactivated Haemophilus parasuis strain 4800
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Intervet International Booxmer, Nīderlande
Date of authorisation/renewal: 08-Dec-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (29-Nov-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (29-Nov-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (29-Nov-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/05/1623-01 1 Polietilēna flakons, 10 deva -
V/MRP/05/1623-02 1 Polietilēna flakons, 25 deva -
V/MRP/05/1623-03 1 Polietilēna flakons, 50 deva -
V/MRP/05/1623-04 6 Stikla flakons, 10 deva -
V/MRP/05/1623-05 6 Stikla flakons, 25 deva -
V/MRP/05/1623-06 6 Stikla flakons, 50 deva -
V/MRP/05/1623-07 12 Stikla flakons, 10 deva -
V/MRP/05/1623-08 12 Stikla flakons, 25 deva -
V/MRP/05/1623-09 12 Stikla flakons, 50 deva -
V/MRP/05/1623-10 1 Stikla flakons, 10 deva -
V/MRP/05/1623-11 1 Stikla flakons, 25 deva -
V/MRP/05/1623-12 1 Stikla flakons, 50 deva -
V/MRP/05/1623-13 6 Polietilēna flakons, 10 deva -
V/MRP/05/1623-14 6 Polietilēna flakons, 25 deva -
V/MRP/05/1623-15 6 Polietilēna flakons, 50 deva -
V/MRP/05/1623-16 12 Polietilēna flakons, 10 deva -
V/MRP/05/1623-17 12 Polietilēna flakons, 25 deva -
V/MRP/05/1623-18 12 Polietilēna flakons, 50 deva -
Vetmedin S 5 mg V/MRP/15/0013 Boehringer Ingelheim Vetmedica GmbH, Vācija 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 Lavet Pharmaceuticals, Ungārija
Date of authorisation/renewal: 02-Jan-2020
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (19-Apr-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (19-Apr-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (19-Apr-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/15/0013-01 5 mg 2 PVH/Al blisteris (necaurspīdīgs), 10 tablete -
V/MRP/15/0013-02 5 mg 5 PVH/Al blisteris (necaurspīdīgs), 10 tablete -
V/MRP/15/0013-03 5 mg 10 PVH/Al blisteris (necaurspīdīgs), 10 tablete -
Vetmedin S 10 mg V/MRP/15/0014 Boehringer Ingelheim Vetmedica GmbH, Vācija 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 Lavet Pharmaceuticals, Ungārija
Date of authorisation/renewal: 02-Jan-2020
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (19-Apr-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (19-Apr-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (19-Apr-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/15/0014-01 10 mg 2 PVH/Al blisteris (necaurspīdīgs), 10 tablete -
V/MRP/15/0014-02 10 mg 5 PVH/Al blisteris (necaurspīdīgs), 10 tablete -
V/MRP/15/0014-03 10 mg 10 PVH/Al blisteris (necaurspīdīgs), 10 tablete -
Pestigon 50 mg V/DCP/12/0047 Norbrook Laboratories (Ireland) Limited, Īrija QP53AX15 cats 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 Norbrook Laboratories Limited, Lielbritānija;Norbrook Laboratories Limited, Lielbritānija;Norbrook Manufacturing Limited, Īrija
Date of authorisation/renewal: 04-Jul-2017
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (23-Mar-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (23-Mar-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (23-Mar-2026)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/12/0047-01 50 mg/deva 1 Plastmasas pipete, 1 deva -
V/DCP/12/0047-02 50 mg/deva 2 Plastmasas pipete, 1 deva -
V/DCP/12/0047-03 50 mg/deva 3 Plastmasas pipete, 1 deva -
V/DCP/12/0047-04 50 mg/deva 4 Plastmasas pipete, 1 deva -
V/DCP/12/0047-05 50 mg/deva 6 Plastmasas pipete, 1 deva -
V/DCP/12/0047-06 50 mg/deva 8 Plastmasas pipete, 1 deva -
V/DCP/12/0047-07 50 mg/deva 12 Plastmasas pipete, 1 deva -
V/DCP/12/0047-08 50 mg/deva 24 Plastmasas pipete, 1 deva -
V/DCP/12/0047-09 50 mg/deva 30 Plastmasas pipete, 1 deva -
V/DCP/12/0047-10 50 mg/deva 60 Plastmasas pipete, 1 deva -
V/DCP/12/0047-11 50 mg/deva 90 Plastmasas pipete, 1 deva -
V/DCP/12/0047-12 50 mg/deva 120 Plastmasas pipete, 1 deva -
V/DCP/12/0047-13 50 mg/deva 150 Plastmasas pipete, 1 deva -
Hymatil 300 mg/ml V/DCP/09/0021 Industrial Veterinaria, S.A., Spānija QJ01FA91 cattle; sheep Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Tilmicosin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Industrial Veterinaria, S.A. - Invesa, Spānija
Date of authorisation/renewal: 02-Oct-2014
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Dec-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Dec-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (03-Dec-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/09/0021-01 300 mg/ml 6 Stikla pudelīte (brūna), 50 ml -
V/DCP/09/0021-02 300 mg/ml 6 Stikla pudelīte (brūna), 100 ml -
V/DCP/09/0021-03 300 mg/ml 6 Stikla pudelīte (brūna), 250 ml -
V/DCP/09/0021-04 300 mg/ml 10 Stikla pudelīte (brūna), 50 ml -
V/DCP/09/0021-05 300 mg/ml 12 Stikla pudelīte (brūna), 50 ml -
V/DCP/09/0021-06 300 mg/ml 10 Stikla pudelīte (brūna), 100 ml -
V/DCP/09/0021-07 300 mg/ml 12 Stikla pudelīte (brūna), 100 ml -
V/DCP/09/0021-08 300 mg/ml 10 Stikla pudelīte (brūna), 250 ml -
V/DCP/09/0021-09 300 mg/ml 12 Stikla pudelīte (brūna), 250 ml -
V/DCP/09/0021-10 300 mg/ml 1 Stikla pudelīte (brūna), 50 ml -
V/DCP/09/0021-11 300 mg/ml 1 Stikla pudelīte (brūna), 100 ml -
V/DCP/09/0021-12 300 mg/ml 1 Stikla pudelīte (brūna), 250 ml -
Histodine 10 mg/ml V/DCP/17/0020 Le Vet Beheer B.V., Nīderlande QR06AB04 cattle Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Chlorphenamine maleate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Produlab Pharma b.v., Nīderlande
Date of authorisation/renewal: 26-May-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 26052022LI (26-May-2022)
Labelling text: [DOCX] 26052022M (26-May-2022)
Summary of product characteristics: [DOCX] 26052022ZA (26-May-2022)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/17/0020-01 10 mg/ml 1 Stikla flakons, 100 ml -
V/DCP/17/0020-02 10 mg/ml 1 Stikla flakons, 250 ml -
V/DCP/17/0020-03 10 mg/ml 1 Polipropilēna flakons, 100 ml -
V/DCP/17/0020-04 10 mg/ml 1 Polipropilēna flakons, 250 ml -

3081 record

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