Veterinary medicinal product register

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Data selected by 71
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
RIMADYL Cattle 50 mg/ml V/MRP/08/1586 Zoetis Belgium S.A., Beļģija QM01AE91 cattle 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 Bela-pharm GmbH&Co.KG, Vācija
Date of authorisation/renewal: 07-Dec-2012
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Mar-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Mar-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (20-Mar-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/08/1586-01 50 mg/ml 1 Stikla flakons, 50 ml -
V/MRP/08/1586-02 50 mg/ml 1 Stikla flakons, 100 ml -
V/MRP/08/1586-03 50 mg/ml 1 Stikla flakons, 250 ml -
Api-Bioxal 62 mg/ml V/MRP/21/0021 Chemicals Laif S.p.A., Itālija QP53AG03 honey bees Vairāk

Medicinal product information

Pharmaceutical form: Bee-hive solution
International name (active substance): Oxalic acid dihydrate
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release Chemifarma S.p.A., Itālija
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [DOCX] 171221M+LI (17-Dec-2021)
Labelling text: [DOCX] 171221M+LI (17-Dec-2021)
Summary of product characteristics: [DOCX] 171221ZA (17-Dec-2021)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/21/0021-01 62 mg/ml 1 ABPE pudele, 500 ml -
V/MRP/21/0021-02 62 mg/ml 1 ABPE konteiners, 5 l -
V/MRP/21/0021-03 62 mg/ml 1 Polietilēna maiss, 5 l -
Synulox 250 mg - V/MRP/09/0025 Zoetis Belgium S.A., Beļģija QJ01CR02 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Amoxicillin trihydrate, Potassium clavulanate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Haupt Pharma Latina S.R.L., Itālija
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 (21-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (21-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (21-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/09/0025-01 250 mg 1 Alumīnija folija blisteris, 10 tablete -
V/MRP/09/0025-02 250 mg 10 Alumīnija folija blisteris, 10 tablete -
V/MRP/09/0025-03 250 mg 25 Alumīnija folija blisteris, 10 tablete -
Synulox 500 mg - V/MRP/09/0026 Zoetis Belgium S.A., Beļģija QJ01CR02 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Amoxicillin trihydrate, Potassium clavulanate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Haupt Pharma Latina S.R.L., Itālija
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 (21-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (21-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (21-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/09/0026-01 500 mg 5 Alumīnija folija blisteris, 2 tablete -
V/MRP/09/0026-02 500 mg 10 Alumīnija folija blisteris, 2 tablete -
V/MRP/09/0026-03 500 mg 50 Alumīnija folija blisteris, 2 tablete -
V/MRP/09/0026-04 500 mg 100 Alumīnija folija blisteris, 2 tablete -
Synulox 50 mg - V/MRP/99/1027 Zoetis Belgium S.A., Beļģija QJ01CR02 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Amoxicillin trihydrate, Potassium clavulanate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Haupt Pharma Latina S.R.L., Itālija
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 (21-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (21-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (21-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/99/1027-01 50 mg 1 Alumīnija folija blisteris, 10 tablete -
V/MRP/99/1027-02 50 mg 10 Alumīnija folija blisteris, 10 tablete -
V/MRP/99/1027-14 50 mg 25 Alumīnija folija blisteris, 10 tablete -
V/MRP/99/1027-15 50 mg 50 Alumīnija folija blisteris, 10 tablete -
DOMOSEDAN GEL 7.6 mg/ml V/DCP/09/0004 Orion Corporation, Somija QN05CM90 horses Vairāk

Medicinal product information

Pharmaceutical form: oromucosal gel
International name (active substance): Detomidine hydrochloride
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Orion Corporation, Somija
Date of authorisation/renewal: 01-Nov-2013
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (06-May-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (06-May-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (06-May-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/09/0004-01 7,6 mg/ml 1 polietilēna šļirce, 3 ml -
Butomidor 10 mg/ml V/MRP/17/0029 VetViva Richter GmbH , Austrija QN02AF01 horses; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Butorphanol tartrate
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release VetViva Richter GmbH , Austrija
Date of authorisation/renewal: 27-Jul-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (12-Aug-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (12-Aug-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (12-Aug-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/17/0029-01 1 Stikla flakons, 10 ml -
V/MRP/17/0029-02 5 Stikla flakons, 10 ml -
V/MRP/17/0029-03 10 Stikla flakons, 10 ml -
V/MRP/17/0029-04 1 Stikla flakons, 50 ml -
Addimag - V/DCP/22/0001 Alfasan Nederland BV, Nīderlande QA12AX cattle Vairāk

Medicinal product information

Pharmaceutical form: solution for infusion
International name (active substance): Calcii gluconas monohydricus, Magnesii chloridum hexahydricum
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bela-pharm GmbH&Co.KG, Vācija;Alfasan Nederland BV, Nīderlande
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 (23-Feb-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (23-Feb-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (23-Feb-2026)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/22/0001-01 1 Polipropilēna pudele, 500 ml -
V/DCP/22/0001-02 1 Polipropilēna pudele, 750 ml -
Addimag - V/DCP/22/0002 Alfasan Nederland BV, Nīderlande QA12AX cattle Vairāk

Medicinal product information

Pharmaceutical form: solution for infusion
International name (active substance): Calcii gluconas monohydricus, Magnesii chloridum hexahydricum
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bela-pharm GmbH&Co.KG, Vācija;Alfasan Nederland BV, Nīderlande
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 (23-Feb-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (23-Feb-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (23-Feb-2026)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/22/0002-01 1 Polipropilēna pudele, 500 ml -
V/DCP/22/0002-02 1 Polipropilēna pudele, 750 ml -
Alfaglandin C 0.250 mg/ml V/MRP/11/0001 Alfasan Nederland BV, Nīderlande QG02AD90 cattle Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Cloprostenol sodium
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Alfasan Nederland BV, Nīderlande
Date of authorisation/renewal: 20-May-2013
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (30-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (30-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (30-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/11/0001-01 0,25 mg/ml 28 Stikla flakons, 20 ml -
V/MRP/11/0001-02 0,25 mg/ml 1 Stikla flakons, 20 ml -
BioBos Mastiguard - V/DCP/24/0068 Bioveta a.s., Čehija QI02AB17 Cattle (heifer); Catlle (cow) Vairāk

Medicinal product information

Pharmaceutical form: suspension for injection
International name (active substance): Escherichia coli, strain 5117, J5, inactivated, Staphylococcus aureus, strain DSM 4910, inactivated
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bioveta a.s., Čehija
Date of authorisation/renewal: 18-Oct-2024
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (18-Oct-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (18-Oct-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (18-Oct-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/24/0068-01 10 Stikla flakons, 5 deva -
V/DCP/24/0068-02 10 Plastmasas flakons, 5 deva -
V/DCP/24/0068-03 1 Stikla flakons, 5 deva -
V/DCP/24/0068-04 1 Plastmasas flakons, 5 deva -
V/DCP/24/0068-05 1 Stikla flakons, 25 deva -
V/DCP/24/0068-06 1 Plastmasas flakons, 25 deva -
V/DCP/24/0068-07 1 Stikla flakons, 50 deva -
V/DCP/24/0068-08 1 Plastmasas flakons, 50 deva -
Canigen DHPPi - V/DCP/16/0014 VIRBAC, Francija QI07AD04 dogs Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and solvent for suspension for injection
International name (active substance): Live attenuated canine distemper virus (CDV) - Lederle strain, Live attenuated canine adenovirus type 2 (CAV-2) - Manhattan strain, Live attenuated canine parvovirus (CPV) - CPV780916 strain, Live attenuated canine parainfluenza virus (CPIV) - Manhattan strain
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release VIRBAC, Francija
Date of authorisation/renewal: 21-Apr-2021
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (11-Aug-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (11-Aug-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (11-Aug-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/16/0014-01 1 Stikla flakons (kartona kastē), 1 deva -
V/DCP/16/0014-02 5 Stikla flakons (kartona kastē), 1 deva -
V/DCP/16/0014-03 10 Stikla flakons (kartona kastē), 1 deva -
V/DCP/16/0014-04 25 Stikla flakons (kartona kastē), 1 deva -
V/DCP/16/0014-05 50 Stikla flakons (kartona kastē), 1 deva -
V/DCP/16/0014-06 100 Stikla flakons (kartona kastē), 1 deva -
V/DCP/16/0014-07 1 Stikla flakons (plastmasas kastē), 1 deva -
V/DCP/16/0014-08 5 Stikla flakons (plastmasas kastē), 1 deva -
V/DCP/16/0014-09 10 Stikla flakons (plastmasas kastē), 1 deva -
V/DCP/16/0014-10 25 Stikla flakons (plastmasas kastē), 1 deva -
V/DCP/16/0014-11 50 Stikla flakons (plastmasas kastē), 1 deva -
V/DCP/16/0014-12 100 Stikla flakons (plastmasas kastē), 1 deva -
Fatroximin Dry Cow 100/5 mg/ml - V/NRP/01/1372 Fatro S.p.A., Itālija QJ51XX01 dry cows Vairāk

Medicinal product information

Pharmaceutical form: intramammary suspension
International name (active substance): Rifaximin
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 (10-Jun-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Jun-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (10-Jun-2024)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/01/1372-01 100 mg/deva 4 Injektors, 1 deva -
V/NRP/01/1372-02 100 mg/deva 12 Injektors, 1 deva -
Bioestrovet 0.250 mg/ml V/DCP/17/0002 Vetoquinol S.A., Francija QG02AD90 cattle Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Cloprostenol sodium
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Vetoquinol S.A., Francija
Date of authorisation/renewal: 20-Dec-2021
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Oct-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (06-Oct-2025)
Summary of product characteristics: [DOC] Zāļu_informācija_ZA_M_LI (06-Oct-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/17/0002-01 1 Stikla flakons, 20 ml -
V/DCP/17/0002-02 1 Stikla flakons, 50 ml -
V/DCP/17/0002-03 1 Stikla flakons, 100 ml -
Cortotic 0.584 mg/ml V/DCP/22/0044 VIRBAC, Francija QS02BA01 dogs Vairāk

Medicinal product information

Pharmaceutical form: Ear spray, solution
International name (active substance): Hydrocortisone aceponate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release VIRBAC, Francija
Date of authorisation/renewal: 30-Nov-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (07-Feb-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (07-Feb-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (07-Feb-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/22/0044-01 1 ABPE pudele, 16 ml -
Flimabend 100 mg/g V/DCP/13/0003 KRKA, d.d., Novo mesto, Slovēnija QP52AC12 pigs; chickens Vairāk

Medicinal product information

Pharmaceutical form: suspension for use in drinking water
International name (active substance): Flubendazole
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release KRKA, d.d., Novo mesto, Slovēnija;TAD Pharma GmbH, Vācija
Date of authorisation/renewal: 28-Nov-2017
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Nov-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Nov-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (16-Nov-2023)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/13/0003-01 100 mg/g 2 Papīra/PE/Al folijas/PE paciņa, 20 g -
V/DCP/13/0003-02 100 mg/g 24 Papīra/PE/Al folijas/PE paciņa, 20 g -
V/DCP/13/0003-03 100 mg/g 2 Papīra/PE/Al folijas/PE paciņa, 50 g -
V/DCP/13/0003-04 100 mg/g 24 Papīra/PE/Al folijas/PE paciņa, 50 g -
V/DCP/13/0003-05 100 mg/g 1 Papīra/PE/Al folijas/PE paciņa, 100 g -
V/DCP/13/0003-06 100 mg/g 5 Papīra/PE/Al folijas/PE paciņa, 100 g -
V/DCP/13/0003-07 100 mg/g 25 Papīra/PE/Al folijas/PE paciņa, 100 g -
V/DCP/13/0003-08 100 mg/g 4 Konteiners, 750 g -
V/DCP/13/0003-09 100 mg/g 6 Konteiners, 750 g -
IZOMITOR 1000 mg/g V/SRP/23/0066 Piramal Critical Care B.V., Nīderlande QN01AB06 guinea pigs; hamsters; chinchilla; ferrets; horses; mouses; rats; dogs; cats; exotic birds; reptiles; gerbils Vairāk

Medicinal product information

Pharmaceutical form: inhalation vapour, liquid
International name (active substance): Isoflurane
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Piramal Critical Care B.V., Nīderlande
Date of authorisation/renewal: 12-Dec-2023
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: SRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (12-Dec-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (12-Dec-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (19-Dec-2025)

Products

ID Strength Package size Primary packaging Labelling
V/SRP/23/0066-01 1 Stikla pudelīte (dzintarkrāsas), 100 ml [PDF] [PDF]
V/SRP/23/0066-02 1 Stikla pudelīte (dzintarkrāsas), 250 ml [PDF] [PDF]
Giraxa 50 mg/g V/DCP/08/1563 KRKA, d.d., Novo mesto, Slovēnija QA07AA10 calves; piglets; chickens Vairāk

Medicinal product information

Pharmaceutical form: powder for oral solution
International name (active substance): Colistin sulfate
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: 20-May-2013
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Dec-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Dec-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (16-Dec-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/08/1563-01 50 mg/g 1 Alumīnija folijas maisiņš, 100 g -
V/DCP/08/1563-02 50 mg/g 1 Alumīnija folijas maisiņš, 1000 g -
V/DCP/08/1563-03 50 mg/g 1 PP konteiners, 100 g -
V/DCP/08/1563-04 50 mg/g 1 PP konteiners, 1000 g -
Tuloxxin 25 mg/ml V/DCP/20/0051 KRKA, d.d., Novo mesto, Slovēnija QJ01FA94 pigs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Tulathromycin
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: 27-Oct-2020
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 171221LI (17-Dec-2021)
Labelling text: [DOCX] 171221M (17-Dec-2021)
Summary of product characteristics: [DOCX] 171221ZA (17-Dec-2021)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/20/0051-01 25 mg/ml 1 Stikla flakons, 50 ml -
V/DCP/20/0051-02 25 mg/ml 1 Stikla flakons, 100 ml -
V/DCP/20/0051-03 25 mg/ml 1 Stikla flakons, 250 ml -
Cefabactin vet 500 mg V/DCP/16/0017 Le Vet Beheer B.V., Nīderlande QJ01DB01 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Cefalexin monohydrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Lelypharma B.V., Nīderlande
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 (22-May-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (22-May-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (22-May-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/16/0017-01 500 mg 1 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0017-02 500 mg 2 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0017-03 500 mg 3 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0017-04 500 mg 4 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0017-05 500 mg 5 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0017-06 500 mg 6 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0017-07 500 mg 7 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0017-08 500 mg 8 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0017-09 500 mg 9 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0017-10 500 mg 10 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0017-11 500 mg 25 PVDH/PE/PVH/Al blisteris, 10 tablete -
V/DCP/16/0017-12 500 mg 10 Kastīte ar blisteri, 10 tablete -

3082 records

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