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
Xylazine 2% 20 mg/ml V/NRP/97/0544 Alfasan International B.V., Nīderlande 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 Alfasan International B.V., Nīderlande
Date of authorisation/renewal: 30-Dec-2009
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 220318LI (09-Apr-2018)
Labelling text: [PDF] 220318M (09-Apr-2018)
Summary of product characteristics: [PDF] 220318ZA (09-Apr-2018)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/97/0544-01 20 mg/ml 1 Stikla (tumša) flakons, 30 ml -
V/NRP/97/0544-02 20 mg/ml 1 Stikla (tumša) flakons, 50 ml -
V/NRP/97/0544-03 20 mg/ml 28 Stikla (tumša) flakons, 30 ml -
V/NRP/97/0544-04 20 mg/ml 15 Stikla (tumša) flakons, 50 ml -
Coliprim 2400 - V/NRP/07/1707 LAVET Pharmaceuticals Ltd., Ungārija QA07AA10 pigs; turkeys; chickens Vairāk

Medicinal product information

Pharmaceutical form: oral powder
International name (active substance): Colistin sulfate
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: [PDF] 220716LI (26-Jul-2016)
Labelling text: [PDF] 220716M (26-Jul-2016)
Summary of product characteristics: [PDF] 220716ZA (26-Jul-2016)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/07/1707-01 120 mg/g 1 Plastmasas konteiners, 1 kg -
V/NRP/07/1707-02 120 mg/g 1 Plastmasas konteiners, 5 kg -
V/NRP/07/1707-03 120 mg/g 1 Papīra maisiņš, 10 kg -
Pen-Strep 20/20 inj.susp. - V/NRP/04/1627 V.M.D. n.v., Beļģija QJ01RA01 cattle; pigs; sheep; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Procaine benzylpenicillin, Dihydrostreptomycin sulphate
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-Feb-2009
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 200217LI (30-May-2017)
Labelling text: [PDF] 200217M (30-May-2017)
Summary of product characteristics: [PDF] 200217ZA (30-May-2017)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/04/1627-01 1 Stikla flakons, 100 ml -
V/NRP/04/1627-02 1 Stikla flakons, 250 ml -
Canaural - V/NRP/96/0293 Dechra Veterinary Products A/S, Dānija QS02CA01 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: ear drops, suspension
International name (active substance): Diethanolamine fusidate, Framycetin sulphate, Nystatin, Prednisolone
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release GENERA Inc., Horvātija
Date of authorisation/renewal: 18-May-2012
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [DOCX] 01082022LI (01-Aug-2022)
Labelling text: [PDF] 071119M (07-Nov-2019)
Summary of product characteristics: [DOCX] 040424ZA (04-Apr-2024)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/96/0293-01 1 Polietilēna flakons, 15 ml [PDF] [PDF]
Mastilex - V/NRP/97/0632 Industrial Veterinaria, S.A., Spānija QJ51RD01 cattle Vairāk

Medicinal product information

Pharmaceutical form: intramammary suspension
International name (active substance): Cefalexin,Gentamicin
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: 13-Jun-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 230210LI (26-Feb-2010)
Labelling text: [PDF] 230110M (26-Feb-2010)
Summary of product characteristics: [PDF] 230210ZA (26-Feb-2010)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/97/0632-01 4 Injektors, 1 deva -
V/NRP/97/0632-02 24 Injektors, 1 deva -
Ketink 100 mg/ml V/DCP/12/0020 Industrial Veterinaria, S.A., 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 Industrial Veterinaria, S.A., Spānija
Date of authorisation/renewal: 29-Dec-2016
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Feb-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Feb-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (06-Feb-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/12/0020-01 100 mg/ml 1 Stikla pudelīte (dzintarkrāsas), 100 ml -
V/DCP/12/0020-02 100 mg/ml 6 Stikla pudelīte (dzintarkrāsas), 100 ml -
V/DCP/12/0020-03 100 mg/ml 10 Stikla pudelīte (dzintarkrāsas), 100 ml -
V/DCP/12/0020-04 100 mg/ml 12 Stikla pudelīte (dzintarkrāsas), 100 ml -
V/DCP/12/0020-05 100 mg/ml 1 Stikla pudelīte (dzintarkrāsas), 250 ml -
V/DCP/12/0020-06 100 mg/ml 6 Stikla pudelīte (dzintarkrāsas), 250 ml -
V/DCP/12/0020-07 100 mg/ml 10 Stikla pudelīte (dzintarkrāsas), 250 ml -
V/DCP/12/0020-08 100 mg/ml 12 Stikla pudelīte (dzintarkrāsas), 250 ml -
Vitamin AD3E pro injectione - V/MRP/19/0038 Bela-pharm GmbH&Co.KG, Vācija QA11JA cattle; pigs; horses; dogs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Retinol palmitate, All-Rac-Alpha-Tocopheryl Acetate, Cholecalciferol
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: MRP
Package leaflet: [DOC] 260122_LI (26-Jan-2022)
Labelling text: [DOC] 260122_M (26-Jan-2022)
Summary of product characteristics: [DOC] 260122_ZA (26-Jan-2022)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/19/0038-01 1 Stikla flakons, 100 ml [PDF] [PDF]
V/MRP/19/0038-02 6 Stikla flakons, 100 ml -
V/MRP/19/0038-03 12 Stikla flakons, 100 ml [PDF] [PDF]
Nanotrim 464,2 mg/g + 100 mg/g - V/DCP/25/0003 Huvepharma NV, Beļģija QJ01EW12 pigs; turkeys; chickens; pre-ruminant cattle Vairāk

Medicinal product information

Pharmaceutical form: powder for use in drinking water/ milk
International name (active substance): Sulfachlorpyridazine sodium, Trimethoprim
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Biovet JSC, Bulgārija
Date of authorisation/renewal: 17-Jan-2025
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (08-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (08-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (08-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/25/0003-01 1 Lamināta paciņa, 100 g -
V/DCP/25/0003-02 1 Lamināta paciņa, 1 kg -
BioBos Respi 2 intranasal - V/MRP/17/0001 Bioveta, a.s., Čehija QI02AD07 cattle Vairāk

Medicinal product information

Pharmaceutical form: nasal spray, lyophilisate and solvent for suspension
International name (active substance): Live attenuated Bovine parainfluenza type 3 virus, strain Bio 23/A, Live attenuated Bovine respiratory syncytial virus, strain Bio 24/A
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bioveta, a.s., Čehija
Date of authorisation/renewal: 01-Aug-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (21-Oct-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (21-Oct-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (21-Oct-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/17/0001-01 1 Stikla flakons, 5 deva -
V/MRP/17/0001-02 5 Stikla flakons, 5 deva -
Soluclin 25 mg/ml V/DCP/23/0012 CP-Pharma Handelsgesellschaft GmbH, Vācija QJ01FF01 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: Oral solution
International name (active substance): Clindamycin 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: 28-Mar-2023
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Nov-2025)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (03-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/23/0012-01 1 Stikla pudele (dzintarkrāsas), 10 ml -
V/DCP/23/0012-02 1 Stikla pudele (dzintarkrāsas), 25 ml -
V/DCP/23/0012-03 1 Stikla pudele (dzintarkrāsas), 50 ml -
TAbic V.H. - V/NRP/10/0032 PHIBRO ANIMAL HEALTH (POLAND) Sp. z o.o., Polija QI01AD06 turkeys; chickens Vairāk

Medicinal product information

Pharmaceutical form: effervescent tablets
International name (active substance): Newcastle disease virus, strain V.H.
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Synoptis Industrial Sp. z o.o., Polija
Date of authorisation/renewal: 27-Oct-2015
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (15-May-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (15-May-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (15-May-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/10/0032-01 5 Alumīnija blisteris, 100 deva -
V/NRP/10/0032-02 10 Alumīnija blisteris, 100 deva -
V/NRP/10/0032-03 5 Alumīnija blisteris, 500 deva -
V/NRP/10/0032-04 10 Alumīnija blisteris, 500 deva -
V/NRP/10/0032-05 5 Alumīnija blisteris, 1000 deva -
V/NRP/10/0032-06 10 Alumīnija blisteris, 1000 deva -
V/NRP/10/0032-07 5 Alumīnija blisteris, 2000 deva -
V/NRP/10/0032-08 10 Alumīnija blisteris, 2000 deva -
V/NRP/10/0032-09 5 Alumīnija blisteris, 2500 deva -
V/NRP/10/0032-10 10 Alumīnija blisteris, 2500 deva -
V/NRP/10/0032-11 5 Alumīnija blisteris, 5000 deva -
V/NRP/10/0032-12 10 Alumīnija blisteris, 5000 deva -
V/NRP/10/0032-13 5 Alumīnija blisteris, 10000 deva -
V/NRP/10/0032-14 10 Alumīnija blisteris, 10000 deva -
Sedachem 20 mg/ml V/MRP/20/0060 Interchemie Werken De Adelaar Eesti AS, Igaunija 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 Interchemie Werken De Adelaar Eesti AS, Igaunija
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [DOCX] 27082025LI (27-Aug-2025)
Labelling text: [DOCX] 231120M (23-Nov-2020)
Summary of product characteristics: [DOCX] 27082025ZA (27-Aug-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/20/0060-01 20 mg/ml 1 Stikla pudele, 50 ml -
V/MRP/20/0060-02 20 mg/ml 5 Stikla pudele, 50 ml -
Catophos - V/DCP/23/0032 CP-Pharma Handelsgesellschaft GmbH, Vācija QA12CX99 cattle; horses; dogs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): BUTAFOSFAN, Cyanocobalamin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release CP-Pharma Handelsgesellschaft GmbH, Vācija
Date of authorisation/renewal: 27-Jun-2023
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Mar-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Mar-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (06-Mar-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/23/0032-01 100 ml 1 Stikla pudele (dzintarkrāsas), 100 ml -
V/DCP/23/0032-02 250 ml 1 Stikla pudele (dzintarkrāsas), 250 ml -
Ceftiomax 50 mg/ml V/MRP/10/0003 Laboratorios Calier, S.A., Spānija QJ01DD90 cattle; pigs Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Ceftiofur
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Laboratorios Calier, S.A., Spānija
Date of authorisation/renewal: 01-Nov-2013
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (08-Jun-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (08-Jun-2026)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (08-Jun-2026)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/10/0003-01 50 mg/ml 1 Stikla flakons, 100 ml -
V/MRP/10/0003-02 50 mg/ml 1 Stikla flakons, 250 ml -
Paracox-5 - V/MRP/06/1674 Intervet International B.V., Nīderlande QI01AN01 chickens Vairāk

Medicinal product information

Pharmaceutical form: suspension for oral suspension
International name (active substance): E. acervulina HP,E. maxima CP,E. maxima MFP,E. mitis HP,E. tenella HP
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Merck Sharp&Dohme Animal Health S.L., Spānija;MSD Animal Health UK Ltd., Lielbritānija
Date of authorisation/renewal: 08-Jun-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 (23-Mar-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/06/1674-01 1 Flakons, 1000 deva -
V/MRP/06/1674-02 1 Flakons, 5000 deva -
Paracox-8 vet. - V/NRP/04/0003 Intervet International B.V., Nīderlande QI01AN01 chickens Vairāk

Medicinal product information

Pharmaceutical form: suspension for oral suspension
International name (active substance): E. acervulina HP,E. maxima CP,E. maxima MFP,E. mitis HP,E. tenella HP,E. praecox HP,E. brunetti HP,E. necatrix HP
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Merck Sharp&Dohme Animal Health S.L., Spānija;MSD Animal Health UK Ltd., Lielbritānija
Date of authorisation/renewal: 09-Jul-2009
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (28-May-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (28-May-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (28-May-2024)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/04/0003-01 1 Flakons, 4 ml;Pudele (šķīdinātājs), 100 ml -
V/NRP/04/0003-02 1 Pudele (šķīdinātājs), 500 ml;Flakons, 20 ml -
Baycox Multi 50 mg/ml V/DCP/16/0033 Elanco Animal Health GmbH, Vācija QP51BC01 cattle; pigs; sheep Vairāk

Medicinal product information

Pharmaceutical form: suspension for oral use
International name (active substance): Toltrazuril
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release KVP Pharma und Veterinär - Produkte GmbH, Vācija
Date of authorisation/renewal: 27-Oct-2021
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (12-Dec-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (12-Dec-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (12-Dec-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/16/0033-01 1 ABPE pudele, 100 ml -
V/DCP/16/0033-02 1 ABPE pudele, 250 ml -
V/DCP/16/0033-03 1 ABPE pudele, 1000 ml -
Floron solution for injection 300 mg/ml - V/NRP/01/1417 KRKA, d.d., Novo mesto, Slovēnija QJ01BA90 cattle; pigs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Florfenicol
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: 19-Jan-2012
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (18-Mar-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (18-Mar-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (18-Mar-2024)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/01/1417-01 300 mg/ml 1 Flakons, 50 ml -
V/NRP/01/1417-02 300 mg/ml 1 Flakons, 100 ml -
Alfacilline 15/15 LA - V/NRP/97/0599 Alfasan International B.V., Nīderlande QJ01CE30 cattle; pigs; sheep; horses; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Procainpenicillin, Benzathine penicillin
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: [DOCX] 080620LI (08-Jun-2020)
Labelling text: [PDF] 220517M (06-Jun-2017)
Summary of product characteristics: [DOCX] 080620ZA (08-Jun-2020)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/97/0599-01 1 Stikla flakons, 100 ml -
Gentamycin 85 mg/ml V/NRP/95/0110 Bela-pharm GmbH&Co.KG, Vācija QJ01GB03 cattle; pigs; horses; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Gentamicin sulphate
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: 30-Dec-2009
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 200617LI (26-Jun-2017)
Labelling text: [PDF] 200617M (26-Jun-2017)
Summary of product characteristics: [PDF] 200617ZA (26-Jun-2017)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/95/0110-01 85 mg/ml 1 Stikla flakons, 100 ml -
V/NRP/95/0110-02 85 mg/ml 6 Stikla flakons, 100 ml -
V/NRP/95/0110-03 85 mg/ml 12 Stikla flakons, 100 ml -

3082 records

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