Veterinary medicinal product register

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Data selected by 93
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
Clavubactin 50/12,5 mg tablet - V/NRP/08/1611 Le Vet B.V., Nīderlande QJ01CR02 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Amoxicillin,Potassium clavulanate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 09-Jun-2014
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 290514LI (09-Jun-2014)
Labelling text: [PDF] 290514M (09-Jun-2014)
Summary of product characteristics: [PDF] 290514ZA (09-Jun-2014)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/08/1611-01 50 mg/12,5 tabl. 5 Alumīnija blisteris, 2 tablete -
V/NRP/08/1611-02 50 mg/12,5 mg 5 Alumīnija blisteris, 4 tablete -
V/NRP/08/1611-03 50 mg/12,5 mg 25 Alumīnija blisteris, 4 tablete -
V/NRP/08/1611-04 50 mg/12,5 mg 50 Alumīnija blisteris, 4 tablete -
V/NRP/08/1611-05 50 mg/12,5 mg 25 Alumīnija blisteris, 10 tablete -
V/NRP/08/1611-06 50 mg/12,5 mg 1 Alumīnija blisteris, 10 tablete -
V/NRP/08/1611-07 50 mg/12,5 mg 10 Alumīnija blisteris, 10 tablete -
V/NRP/08/1611-08 50 mg/12,5 mg 50 Alumīnija blisteris, 2 tablete -
Clavubactin 250/62,5 mg tablet - V/NRP/08/1612 Le Vet B.V., Nīderlande QJ01CR02 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Amoxicillin,Potassium clavulanate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 09-Jun-2014
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 290514LI (09-Jun-2014)
Labelling text: [PDF] 290514M (09-Jun-2014)
Summary of product characteristics: [PDF] 290514ZA (09-Jun-2014)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/08/1612-01 250 mg/62,5 mg 5 Alumīnija blisteris, 2 tablete -
V/NRP/08/1612-02 250 mg/62,5 mg 5 Alumīnija blisteris, 4 tablete -
V/NRP/08/1612-03 250 mg/62,5 mg 10 Alumīnija blisteris, 10 tablete -
V/NRP/08/1612-05 250 mg/62,5 mg 25 Alumīnija blisteris, 10 tablete -
V/NRP/08/1612-06 250 mg/62,5 mg 25 Alumīnija blisteris, 4 tablete -
V/NRP/08/1612-07 250 mg/62,5 mg 50 Alumīnija blisteris, 4 tablete -
V/NRP/08/1612-08 250 mg/62,5 mg 1 Alumīnija blisteris, 10 tablete -
V/NRP/08/1612-09 250 mg/62,5 mg 50 Alumīnija blisteris, 2 tablete -
Clavubactin 500/125 mg tablet - V/NRP/08/1613 Le Vet B.V., Nīderlande QJ01CR02 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Amoxicillin,Potassium clavulanate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
Date of authorisation/renewal: 09-Jun-2014
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 290514LI (09-Jun-2014)
Labelling text: [PDF] 290514M (09-Jun-2014)
Summary of product characteristics: [PDF] 290514ZA (09-Jun-2014)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/08/1613-01 500 mg/125 mg 5 Alumīnija blisteris, 2 tablete -
V/NRP/08/1613-02 500 mg/125 mg 5 Alumīnija blisteris, 4 tablete -
V/NRP/08/1613-03 500 mg/125 mg 25 Alumīnija blisteris, 4 tablete -
V/NRP/08/1613-04 500 mg/125 mg 50 Alumīnija blisteris, 4 tablete -
V/NRP/08/1613-05 500 mg/125 mg 25 Alumīnija blisteris, 10 tablete -
V/NRP/08/1613-06 500 mg/125 mg 1 Alumīnija blisteris, 10 tablete -
V/NRP/08/1613-07 500 mg/125 mg 10 Alumīnija blisteris, 10 tablete -
V/NRP/08/1613-08 500 mg/125 mg 50 Alumīnija blisteris, 2 tablete -
Atiquine P50 500 mg/g V/NRP/02/1530 Fatro S.p.A., Itālija QJ01MB07 birds; fish Vairāk

Medicinal product information

Pharmaceutical form: oral powder
International name (active substance): Flumequine
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Fatro S.p.A., Itālija
Date of authorisation/renewal: 15-Jul-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 191015LI (21-Oct-2015)
Labelling text: [PDF] 191015M (21-Oct-2015)
Summary of product characteristics: [PDF] 191015ZA (21-Oct-2015)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/02/1530-01 500 mg/g 1 Plastikāta konteiners, 1 kg -
Cevac Mass L - V/MRP/16/0006 Ceva-Phylaxia Veterinary Biologicals Co. Ltd., Ungārija QI01AD07 chickens Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate for oculonasal suspension
International name (active substance): Live, attenuated infectious bronchitis virus, Massachusetts B-48 strain
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: 25-Feb-2021
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [DOCX] 290617LI (25-Feb-2021)
Labelling text: [DOCX] 290617M (25-Feb-2021)
Summary of product characteristics: [DOCX] 290617ZA (25-Feb-2021)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/16/0006-01 1 Stikla flakons, 1000 deva -
V/MRP/16/0006-02 1 Stikla flakons, 2500 deva -
V/MRP/16/0006-03 1 Stikla flakons, 5000 deva -
V/MRP/16/0006-04 10 Stikla flakons, 1000 deva -
V/MRP/16/0006-05 10 Stikla flakons, 2500 deva -
V/MRP/16/0006-06 10 Stikla flakons, 5000 deva -
V/MRP/16/0006-07 20 Stikla flakons, 1000 deva -
V/MRP/16/0006-08 20 Stikla flakons, 2500 deva -
V/MRP/16/0006-09 20 Stikla flakons, 5000 deva -
LV Macrolan WS 1000 mg/g V/NRP/15/0023 Interchemie Werken De Adelaar Eesti AS, Igaunija QJ01FA90 kids; pigs; turkeys; calves; lambs; chickens Vairāk

Medicinal product information

Pharmaceutical form: powder for use in drinking water
International name (active substance): Tylosin tartrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Interchemie Werken De Adelaar Eesti AS, Igaunija
Date of authorisation/renewal: 01-Jul-2020
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [DOCX] 01072020LI (01-Jul-2020)
Labelling text: [DOCX] 01072020M (01-Jul-2020)
Summary of product characteristics: [DOCX] 01072020ZA (01-Jul-2020)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/15/0023-01 1000 mg/g 1 ABPE pudele, 500 g -
V/NRP/15/0023-02 1000 mg/g 1 Pudele, 1000 g -
V/NRP/15/0023-03 1000 mg/g 1 Folijas paciņa, 100 g -
Doxylin 100% - V/MRP/13/0053 Dopharma Research B.V., Nīderlande QJ01AA02 pigs; calves Vairāk

Medicinal product information

Pharmaceutical form: Powder for use in drinking water/milk
International name (active substance): Doxycyclin hyclate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Dopharma B.V., Nīderlande
Date of authorisation/renewal: 30-Jan-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (15-Jan-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (15-Jan-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (15-Jan-2026)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/13/0053-01 1000 mg/g 1 Polipropilēna konteiners, 1 kg -
V/MRP/13/0053-02 1000 mg/g 1 Polietilēna spainis, 1 kg -
V/MRP/13/0053-03 1000 mg/g 1 Polietilēna spainis, 2 kg -
V/MRP/13/0053-04 1000 mg/g 1 Polietilēna spainis, 5 kg -
V/MRP/13/0053-05 1000 mg/g 1 Polipropilēna konteiners, 100 g -
Avinew NEO - V/NRP/16/0003 Boehringer Ingelheim Animal Health France SCS , Francija QI01AD06 chickens Vairāk

Medicinal product information

Pharmaceutical form: effervescent tablets for suspension
International name (active substance): Live Newcastle Disease virus, strain VG/GA-AVINEW
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release Boehringer Ingelheim Animal Health France SCS, Francija
Date of authorisation/renewal: 27-Oct-2020
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [DOCX] 271020_LI (27-Oct-2020)
Labelling text: [DOCX] 271020_M (27-Oct-2020)
Summary of product characteristics: [DOCX] 271020_ZA (27-Oct-2020)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/16/0003-01 10 Blisteris, 1000 deva -
V/NRP/16/0003-02 100 Blisteris, 1000 deva -
V/NRP/16/0003-03 10 Blisteris, 2000 deva -
V/NRP/16/0003-04 100 Blisteris, 2000 deva -
Biocan Novel DHPPi - V/DCP/14/0049 Bioveta, a.s., Čehija QI07AD04 dogs Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and solvent for suspension for injection
International name (active substance): Canine Parainfluenza virus, strain CPiV2-Bio15, Canine Adenovirus Type 2, strain CAV2-Bio 13, Canine Parvovirus Type 2, strain CPV-2b-Bio 12/B, Canine Distemper virus, strain CDV Bio 11/A
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bioveta, a.s., Čehija
Date of authorisation/renewal: 30-Sep-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (24-Mar-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (24-Mar-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (24-Mar-2026)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/14/0049-01 10 Stikla flakons, 1 deva [PDF] [PDF] [PDF]
V/DCP/14/0049-02 25 Stikla flakons, 1 deva -
V/DCP/14/0049-03 50 Stikla flakons, 1 deva -
Cortico Veyxin 10 mg/ml V/DCP/18/0046 Veyx-Pharma GmbH, Vācija QH02AB06 cattle; horses; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Prednisolone acetate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Veyx-Pharma GmbH, Vācija
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] 021018LI (02-Oct-2018)
Labelling text: [PDF] 021018M (02-Oct-2018)
Summary of product characteristics: [PDF] 021018ZA (02-Oct-2018)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/18/0046-01 10 mg/ml 1 Stikla flakons, 100 ml -
V/DCP/18/0046-02 10 mg/ml 6 Stikla flakons, 100 ml -
V/DCP/18/0046-03 10 mg/ml 12 Stikla flakons, 100 ml -
Rispoval IBR-Marker Vivum - V/MRP/08/1584 Zoetis Belgium S.A., Beļģija QI02AD01 cattle Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and solvent for suspension for injection
International name (active substance): Live, attenuated bovine herpes virus
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 (28-Jul-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (28-Jul-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (28-Jul-2023)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/08/1584-02 1 Stikla pudelīte, 10 deva -
V/MRP/08/1584-03 1 Stikla pudelīte, 50 deva -
Versifel CVR - V/NRP/10/0014 Zoetis Belgium S.A., Beļģija QI06AD04 cats Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and solvent for solution for injection
International name (active substance): Live, attenuated feline calici virus,Feline rhinotracheitis virus,Attenuated feline panleucopenia virus
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Zoetis Belgium S.A., Beļģija
Date of authorisation/renewal: 22-Dec-2014
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (19-Oct-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (19-Oct-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (19-Oct-2023)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/10/0014-01 10 Stikla flakons, 1 deva -
V/NRP/10/0014-02 25 Stikla flakons, 1 deva -
V/NRP/10/0014-03 100 Stikla flakons, 1 deva -
Pen & Strep - V/NRP/96/0445 Norbrook Laboratories (Ireland) Limited, Īrija QJ01RA01 cattle; pigs; sheep; horses Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Procainpenicillin, Dihydrostreptomycin sulphate
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: 14-Aug-2012
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (05-Jan-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (05-Jan-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (05-Jan-2026)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/96/0445-01 1 Stikla flakons, 50 ml -
V/NRP/96/0445-02 1 Stikla flakons, 100 ml -
Sporimune 50 mg/ml V/DCP/14/0041 Le Vet Beheer B.V., Nīderlande 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 Produlab Pharma b.v., Nīderlande
Date of authorisation/renewal: 04-Dec-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (12-Feb-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (12-Feb-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (05-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/14/0041-01 50 mg/ml 1 Stikla pudele (brūna), 25 ml -
V/DCP/14/0041-02 50 mg/ml 1 Stikla pudele (brūna), 50 ml -
V/DCP/14/0041-03 50 mg/ml 1 Stikla pudele (brūna), 100 ml -
Novasul 500 mg/ml V/NRP/97/0557 VetViva Richter GmbH , Austrija QN02BB02 cattle; pigs; horses; dogs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Metamizole sodium monohydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release VetViva Richter GmbH , Austrija
Date of authorisation/renewal: 20-May-2013
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [DOCX] 10052023_LI (10-May-2023)
Labelling text: [DOCX] 23012023_M (23-Jan-2023)
Summary of product characteristics: [DOCX] 23012023_ZA (23-Jan-2023)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/97/0557-01 500 mg/ml 1 Stikla pudelīte (brūna), 100 ml -
Bimectin 18.7 mg/g V/NRP/04/1631 Bimeda Animal Health Limited, Īrija QP54AA01 horses Vairāk

Medicinal product information

Pharmaceutical form: paste for oral use
International name (active substance): Ivermectin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release PROVET S.A., Grieķija
Date of authorisation/renewal: 09-Mar-2009
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (08-Apr-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (08-Apr-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (08-Apr-2026)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/04/1631-01 18,7 mg/g 1 Šļirce, 6,42 g -
Carpcoat 8 mg V/DCP/25/0065 Alfasan Nederland BV, Nīderlande QM01AE91 dogs Vairāk

Medicinal product information

Pharmaceutical form: film-coated tablets
International name (active substance): Carprofen
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: 06-Nov-2025
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (06-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/25/0065-01 1 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0065-02 2 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0065-03 3 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0065-04 4 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0065-05 5 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0065-06 6 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0065-07 7 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0065-08 8 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0065-09 9 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0065-10 10 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0065-11 12 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0065-12 25 PVH/PE/PVDH-Al blisteris, 10 tablete -
Carpcoat 20 mg V/DCP/25/0066 Alfasan Nederland BV, Nīderlande QM01AE91 dogs Vairāk

Medicinal product information

Pharmaceutical form: film-coated tablets
International name (active substance): Carprofen
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: 06-Nov-2025
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (06-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/25/0066-01 1 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0066-02 2 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0066-03 3 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0066-04 4 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0066-05 5 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0066-06 6 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0066-07 7 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0066-08 8 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0066-09 9 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0066-10 10 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0066-11 12 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0066-12 25 PVH/PE/PVDH-Al blisteris, 10 tablete -
Carpcoat 40 mg V/DCP/25/0067 Alfasan Nederland BV, Nīderlande QM01AE91 dogs Vairāk

Medicinal product information

Pharmaceutical form: film-coated tablets
International name (active substance): Carprofen
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: 06-Nov-2025
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (06-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/25/0067-01 1 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0067-02 2 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0067-03 3 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0067-04 4 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0067-05 5 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0067-06 6 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0067-07 7 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0067-08 8 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0067-09 9 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0067-10 10 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0067-11 12 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0067-12 25 PVH/PE/PVDH-Al blisteris, 10 tablete -
Carpcoat 80 mg V/DCP/25/0068 Alfasan Nederland BV, Nīderlande QM01AE91 dogs Vairāk

Medicinal product information

Pharmaceutical form: film-coated tablets
International name (active substance): Carprofen
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: 06-Nov-2025
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (06-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/25/0068-01 1 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0068-02 2 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0068-03 3 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0068-04 4 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0068-05 5 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0068-06 6 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0068-07 7 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0068-08 8 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0068-09 9 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0068-10 10 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0068-11 12 PVH/PE/PVDH-Al blisteris, 10 tablete -
V/DCP/25/0068-12 25 PVH/PE/PVDH-Al blisteris, 10 tablete -

3082 records

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