Veterinary medicinal product register

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Data selected by 820
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
Rilexine 150 mg/ml V/NRP/07/1691 Virbac S.A., Francija QJ01DB01 cattle Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Cefalexin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Virbac S.A., Francija
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 (28-Aug-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (28-Aug-2025)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (28-Aug-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/07/1691-01 150 mg/ml 1 Stikla flakons, 100 ml -
V/NRP/07/1691-02 150 mg/ml 1 Stikla flakons, 250 ml -
VeteCorH 1000 IU/ml V/DCP/25/0043 Laboratorios Calier, S.A., Spānija QG03GA01 cattle; pigs; sheep; goats; horses; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and solvent for solution for injection
International name (active substance): GONADOTROPHIN, CHORIONIC PH. EUR.
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Laboratorios Calier, S.A., Spānija
Date of authorisation/renewal: 06-Jun-2025
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Jun-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Jun-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (06-Jun-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/25/0043-01 1 Stikla flakons (kartona kastē); satur liofilizētu granulu, 5000 IU;Stikla flakons (šķīdinātājs kartona kastītē), 5 ml -
V/DCP/25/0043-02 2 Stikla flakons (kartona kastē); satur liofilizētu granulu, 5000 IU;Stikla flakons (šķīdinātājs kartona kastītē), 5 ml -
V/DCP/25/0043-03 5 Stikla flakons (kartona kastē); satur liofilizētu granulu, 5000 IU;Stikla flakons (šķīdinātājs kartona kastītē), 5 ml -
V/DCP/25/0043-04 1 Stikla flakons (liofilizāts), 5000 IU;Stikla flakons (šķīdinātājs stikla flakonā), 5 ml -
V/DCP/25/0043-05 2 Stikla flakons (liofilizāts), 5000 IU;Stikla flakons (šķīdinātājs stikla flakonā), 5 ml -
V/DCP/25/0043-06 5 Stikla flakons (liofilizāts), 5000 IU;Stikla flakons (šķīdinātājs stikla flakonā), 5 ml -
Parofor 70000 IU/g V/DCP/14/0058 Huvepharma NV, Beļģija QA07AA06 pigs; pre-ruminant cattle Vairāk

Medicinal product information

Pharmaceutical form: Powder for use in drinking water/milk
International name (active substance): Paromomycin sulfate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Biovet Joint Stock Company., Bulgārija
Date of authorisation/renewal: 01-Aug-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Feb-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (26-Feb-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (26-Feb-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/14/0058-01 70 mg/g 1 Papīra/PE/Al folijas/PE paciņa, 1 kg -
V/DCP/14/0058-02 70 mg/g 1 Papīra/PE/Al folijas/PE paciņa, 250 g -
V/DCP/14/0058-03 70 mg/g 1 Papīra/PE/Al folijas/PE paciņa, 500 g -
V/DCP/14/0058-04 70 mg/g 40 PE/AL/PP paciņa, 25 g -
Biocatalin - V/NRP/02/1496 Fatro S.p.A., Itālija QA11JC cattle; pigs; sheep; horses; dogs; cats; rabbits Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Vitamin B 12,Vitamin B1,Vitamin B2,Vitamin B6,Liver and yeast hydrolysates,Nicotinamide,Pantothenic acid
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Fatro S.p.A., Itālija
Date of authorisation/renewal: 13-Jun-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Aug-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Aug-2024)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (27-Aug-2024)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/02/1496-01 1 Flakons, 100 ml -
Metabolase - V/NRP/01/1378 Fatro S.p.A., Itālija QA11JC cattle; pigs; sheep; goats; horses; dogs; cats; rabbits; buffalo Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): L-carnitine hydrochloride, Thiotic acid, Pyridoxine hydrochloride, Cyanocobalamin, D-L Acetylmethionine, L-Arginine, L-ornithine hydrochloride, L-citrulline, L-Lysine hydrochloride, Glycine, Aspartic acid, Glutamic acid, Fructose, Sorbitol
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Fatro S.p.A., Itālija
Date of authorisation/renewal: 04-Jul-2011
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Aug-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Aug-2024)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (27-Aug-2024)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/01/1378-01 1 Flakons, 250 ml -
V/NRP/01/1378-02 1 Flakons, 500 ml -
Canigen CHPPi/LR - V/NRP/00/1234 Virbac S.A., Francija QI07AJ06 dogs Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and suspension for suspension for injection
International name (active substance): Inactivated Leptospira icterohaemorrhagiae,Leptospira canicola,Live Canine distemper virus,Live canine parvovirus strain,Live Canine adenovirus type 2 (CAV2), strain Manhattan LPV3,Live canine parainfluenza viruss,Inactivated Rabies suspension
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Virbac S.A., Francija
Date of authorisation/renewal: 09-Jul-2010
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Jan-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Jan-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (10-Jan-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/00/1234-01 1 Stikla flakons (plastmasas kastē), 1 deva -
V/NRP/00/1234-02 10 Stikla flakons (plastmasas kastē), 1 deva -
V/NRP/00/1234-03 50 Stikla flakons (plastmasas kastē), 1 deva -
V/NRP/00/1234-04 100 Stikla flakons (plastmasas kastē), 1 deva -
V/NRP/00/1234-05 1 Stikla flakons (kartona kastē), 1 deva -
V/NRP/00/1234-06 10 Stikla flakons (kartona kastē), 1 deva -
V/NRP/00/1234-07 50 Stikla flakons (kartona kastē), 1 deva -
V/NRP/00/1234-08 100 Stikla flakons (kartona kastē), 1 deva -
Cefaximin-L - V/NRP/01/1375 Fatro S.p.A., Itālija QJ51RD34 cows Vairāk

Medicinal product information

Pharmaceutical form: Intramammary emulsion
International name (active substance): Rifaximin, Cephacetrile sodium
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Fatro S.p.A., Itālija
Date of authorisation/renewal: 04-Jul-2011
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [DOCX] 23022022LI (23-Feb-2022)
Labelling text: [DOCX] 23022022M (23-Feb-2022)
Summary of product characteristics: [DOCX] 23022022ZA (23-Feb-2022)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/01/1375-01 4 Alumīnija balons, 1 deva -
Rifen 100 mg/ml V/MRP/10/0005 VetViva Richter GmbH , Austrija 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 VetViva Richter GmbH , Austrija
Date of authorisation/renewal: 26-Feb-2013
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (01-Oct-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (01-Oct-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (01-Oct-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/10/0005-01 100 mg/ml 1 Stikla pudelīte (brūna), 50 ml -
V/MRP/10/0005-02 100 mg/ml 10 Stikla pudelīte (brūna), 100 ml -
V/MRP/10/0005-03 100 mg/ml 10 Stikla pudelīte (brūna), 50 ml -
V/MRP/10/0005-04 100 mg/ml 1 Stikla pudelīte (brūna), 100 ml -
Animeloxan 20 mg/ml V/MRP/19/0057 aniMedica GmbH, Vācija QM01AC06 cattle; pigs; horses Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Meloxicam
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release aniMedica GmbH, Vācija;Industrial Veterinaria, S.A., Spānija;aniMedica Herstellungs GmbH, Vācija
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 (09-Dec-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (09-Dec-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (09-Dec-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/19/0057-01 20 mg/ml 1 Stikla flakons, 50 ml -
V/MRP/19/0057-02 20 mg/ml 1 Stikla flakons, 100 ml -
V/MRP/19/0057-03 20 mg/ml 12 Stikla flakons, 50 ml -
V/MRP/19/0057-04 20 mg/ml 12 Stikla flakons, 100 ml -
Betafuse - V/DCP/16/0028 Norbrook Laboratories (Ireland) Limited, Īrija QD07CC01 dogs Vairāk

Medicinal product information

Pharmaceutical form: gel
International name (active substance): Betamethasone valerate,Fusidic acid
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: 11-Aug-2021
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Jan-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Jan-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (17-Jan-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/16/0028-01 1 Alumīnija tūbiņa, 15 g -
V/DCP/16/0028-02 1 Alumīnija tūbiņa, 30 g -
Vitamin E + Selen vet - V/NRP/05/1523 V.M.D. n.v., Beļģija QA11JB cattle (calf); pigs; sheep Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Vitamine E-tocopherol acetate, Sodium selenite anhydrous
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release V.M.D. n.v., Beļģija
Date of authorisation/renewal: 09-Mar-2010
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (24-Feb-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (24-Feb-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (24-Feb-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/05/1523-01 100 mg/ml 1 Flakons, 50 ml -
V/NRP/05/1523-02 100 mg/ml 1 Flakons, 100 ml -
Nobilis Reo 1133 - V/NRP/95/0166 Intervet International B.V., Nīderlande QI01AD10 chickens Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and solvent for suspension for injection
International name (active substance): Live Reovirus
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Intervet International B.V., Nīderlande
Date of authorisation/renewal: 15-Oct-2010
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (05-Mar-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (05-Mar-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (05-Mar-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/95/0166-02 10 Stikla flakons, 1000 deva -
Hypophysin LA 70 µg/ml V/DCP/14/0027 Veyx-Pharma GmbH, Vācija QH01BB03 cattle; pigs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Carbetocin
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: 03-Jul-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 040719LI (12-Aug-2025)
Labelling text: [PDF] 040719M (04-Jul-2019)
Summary of product characteristics: [PDF] 040719ZA (04-Jul-2019)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/14/0027-01 1 Stikla flakons, 10 ml -
V/DCP/14/0027-02 1 Stikla flakons, 20 ml -
V/DCP/14/0027-03 1 Stikla flakons, 50 ml -
Hypophysin LA 35 µg/ml V/DCP/14/0026 Veyx-Pharma GmbH, Vācija QH01BB03 cattle; pigs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Carbetocin
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: 03-Jul-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 040719LI (12-Aug-2025)
Labelling text: [PDF] 040719M (04-Jul-2019)
Summary of product characteristics: [DOCX] 040719ZA (04-Jul-2019)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/14/0026-01 35 µg/ml 1 Stikla flakons, 10 ml -
V/DCP/14/0026-02 35 µg/ml 1 Stikla flakons, 20 ml -
V/DCP/14/0026-03 35 µg/ml 1 Stikla flakons, 50 ml -
V/DCP/14/0026-05 35 µg/ml 1 Stikla flakons, 100 ml -
Maprelin 75 µg/ml V/MRP/09/0015 Veyx-Pharma GmbH, Vācija QH01CA pigs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Peforelin
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: 03-Oct-2013
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [DOCX] 300913LI (12-Aug-2025)
Labelling text: [PDF] 300913M (03-Oct-2013)
Summary of product characteristics: [PDF] 300913ZA (03-Oct-2013)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/09/0015-01 75 µg/ml 1 Stikla pudelīte, 10 ml -
V/MRP/09/0015-02 75 µg/ml 6 Stikla pudelīte, 10 ml -
V/MRP/09/0015-03 75 µg/ml 1 Stikla pudelīte, 50 ml -
V/MRP/09/0015-04 75 µg/ml 1 Stikla pudelīte, 100 ml -
Gonavet Veyx 50 µg/ml V/DCP/15/0003 Veyx-Pharma GmbH, Vācija QH01CA01 cattle; pigs; horses Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Gonadorelin
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: 28-Apr-2020
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 270215LI (12-Aug-2025)
Labelling text: [DOCX] 270215M (28-Apr-2020)
Summary of product characteristics: [DOCX] 270215ZA (28-Apr-2020)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/15/0003-01 50 µg/ml 1 Stikla flakons, 10 ml -
V/DCP/15/0003-02 50 µg/ml 1 Stikla flakons, 20 ml -
V/DCP/15/0003-03 50 µg/ml 1 Stikla flakons, 50 ml -
Spasmalgan compositum - V/DCP/20/0037 Veyx-Pharma GmbH, Vācija QA03DB04 cattle; pigs; horses; dogs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Metamizole sodium monohydrate, Hyoscine butylbromide
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: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 03072020LI (12-Aug-2025)
Labelling text: [DOCX] 03072020M (03-Jul-2020)
Summary of product characteristics: [DOCX] 26012022ZA (26-Jan-2022)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/20/0037-01 500 mg/4 ml 1 Stikla flakons, 10 ml -
V/DCP/20/0037-02 500 mg/4 ml 1 Stikla flakons, 100 ml -
Sensiblex 40 mg/ml V/DCP/17/0026 Veyx-Pharma GmbH, Vācija QG02CX90 cattle Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Denaverine hydrochloride
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-Jul-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 27072022LI (12-Aug-2025)
Labelling text: [DOCX] 27072022M (27-Jul-2022)
Summary of product characteristics: [DOCX] 27092022ZA (27-Sep-2022)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/17/0026-01 40 mg/ml 1 Stikla flakons, 10 ml -
V/DCP/17/0026-02 40 mg/ml 1 Stikla flakons, 50 ml -
Vetospirin 1000 mg/g V/DCP/19/0061 V.M.D. n.v., Beļģija QN02BA04 cattle; pigs Vairāk

Medicinal product information

Pharmaceutical form: Powder for use in drinking water/milk
International name (active substance): Sodium salicylate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release V.M.D. n.v., Beļģija
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 (21-Aug-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (21-Aug-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (21-Aug-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/19/0061-01 10 Polietilēna maisiņš, 100 g -
V/DCP/19/0061-02 1 Polietilēna maisiņš, 1 kg -
V/DCP/19/0061-03 1 Polietilēna maisiņš, 5 kg -
INTRAMAR Lacto 200 mg + 50 mg + 10 mg - V/DCP/25/0006 Bioveta a.s., Čehija QJ51RV01 cattle (lactating cows) Vairāk

Medicinal product information

Pharmaceutical form: intramammary suspension
International name (active substance): Amoxicillin trihydrate, Potassium clavulanate, Prednisolone
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bioveta, a.s., Čehija
Date of authorisation/renewal: 14-Feb-2025
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (14-Feb-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (14-Feb-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (14-Feb-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/25/0006-01 24 Injektors, 4,5 ml -
V/DCP/25/0006-02 24 Injektors (un dezinfekcijas salvetes), 4,5 ml -

3081 record

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