Veterinary medicinal product register

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Data selected by 596
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
LV Butasal-100 - V/NRP/13/0018 UAB "Interchemie werken "De Adelaar" LT", Lietuva QA12CX99 cattle; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Cyanocobalamin,Butaphosphan
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: 02-Feb-2018
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] 27092019LI (27-Sep-2019)
Labelling text: [PDF] 27092019M (27-Sep-2019)
Summary of product characteristics: [PDF] 27092019ZA (27-Sep-2019)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/13/0018-01 100 mg/ml 1 Stikla (tumša) flakons, 50 ml -
V/NRP/13/0018-02 100 mg/ml 1 Stikla (tumša) flakons, 100 ml -
LV Glucortin-20 2 mg/ml V/NRP/12/0040 Interchemie werken „De Adelaar“ LT, Lietuva QH02AB02 cattle; pigs; goats; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Dexamethasone sodium phosphate
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: 04-Jul-2017
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [DOCX] 26102021LI (26-Oct-2021)
Labelling text: [DOCX] 26102021M (26-Oct-2021)
Summary of product characteristics: [DOCX] 26102021ZA (26-Oct-2021)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/12/0040-01 2 mg/ml 1 Stikla pudele ar Al vāciņu, 50 ml -
Cazitel Plus - V/MRP/09/0029 Chanelle Pharmaceuticals Manufacturing Ltd., Īrija QP52AA51 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Praziquantel, Pyrantel embonate, Febantel
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release Chanelle Pharmaceuticals Manufacturing Ltd., Īrija
Date of authorisation/renewal: 08-Apr-2014
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (30-May-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (30-May-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (25-Jul-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/09/0029-01 1 Blisteris, 2 tablete -
V/MRP/09/0029-02 2 Blisteris, 2 tablete -
V/MRP/09/0029-03 3 Blisteris, 2 tablete -
V/MRP/09/0029-04 1 Blisteris, 8 tablete -
V/MRP/09/0029-05 5 Blisteris, 2 tablete -
V/MRP/09/0029-06 6 Blisteris, 2 tablete -
V/MRP/09/0029-07 7 Blisteris, 2 tablete -
V/MRP/09/0029-08 2 Blisteris, 8 tablete -
V/MRP/09/0029-09 9 Blisteris, 2 tablete -
V/MRP/09/0029-10 10 Blisteris, 2 tablete -
V/MRP/09/0029-11 3 Blisteris, 8 tablete -
V/MRP/09/0029-12 14 Blisteris, 2 tablete -
V/MRP/09/0029-13 15 Blisteris, 2 tablete -
V/MRP/09/0029-14 4 Blisteris, 8 tablete -
V/MRP/09/0029-15 18 Blisteris, 2 tablete -
V/MRP/09/0029-16 5 Blisteris, 8 tablete -
V/MRP/09/0029-17 21 Blisteris, 2 tablete -
V/MRP/09/0029-18 22 Blisteris, 2 tablete -
V/MRP/09/0029-19 6 Blisteris, 8 tablete -
V/MRP/09/0029-20 25 Blisteris, 2 tablete -
Procapen Injector 3 g V/DCP/12/0034 aniMedica GmbH, Vācija QJ51CE09 cattle Vairāk

Medicinal product information

Pharmaceutical form: intramammary suspension
International name (active substance): Procaine benzylpenicillin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release aniMedica GmbH, Vācija;Industrial Veterinaria, S.A., Spānija
Date of authorisation/renewal: 04-Apr-2018
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (30-May-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (30-May-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (30-May-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/12/0034-01 3 g/deva 24 Injektors, 1 deva -
PGF Veyx 0.0875 mg/ml V/DCP/12/0038 Veyx-Pharma GmbH, Vācija QG02AD90 cattle; pigs 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 Veyx-Pharma GmbH, Vācija;Veyx-Pharma B.V., Nīderlande
Date of authorisation/renewal: 03-Oct-2017
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Jun-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Jun-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (12-Aug-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/12/0038-01 0,0875 mg/ml 1 Stikla pudelīte, 10 ml -
V/DCP/12/0038-02 0,0875 mg/ml 1 Stikla pudelīte, 20 ml -
V/DCP/12/0038-03 0,0875 mg/ml 1 Stikla pudelīte, 50 ml -
PGF Veyx forte 0.250 mg/ml V/DCP/12/0039 Veyx-Pharma GmbH, Vācija QG02AD90 cattle; pigs 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 Veyx-Pharma GmbH, Vācija;Veyx-Pharma B.V., Nīderlande
Date of authorisation/renewal: 03-Oct-2017
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Jun-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (16-Jun-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (12-Aug-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/12/0039-01 0,25 mg/ml 1 Stikla pudelīte, 10 ml -
V/DCP/12/0039-02 0,25 mg/ml 1 Stikla pudelīte, 20 ml -
V/DCP/12/0039-03 0,25 mg/ml 1 Stikla pudelīte, 50 ml -
BIOSUIS M.hyo - V/MRP/13/0001 Bioveta, a.s., Čehija QI09AB13 pigs Vairāk

Medicinal product information

Pharmaceutical form: emulsion for injection
International name (active substance): Inactivated Mycoplasma hyopneumoniae
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bioveta, a.s., Čehija
Date of authorisation/renewal: 04-Oct-2016
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (02-Apr-2026)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (02-Apr-2026)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (02-Apr-2026)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/13/0001-01 10 Stikla flakons (kartona kastē), 5 deva -
V/MRP/13/0001-02 1 Stikla flakons (kartona kastē), 50 deva -
V/MRP/13/0001-03 1 ABPE pudele kartona kastē, 125 deva -
V/MRP/13/0001-04 10 Stikla flakons (plastmasas kastē), 5 deva -
V/MRP/13/0001-05 1 ABPE flakons (kartona kastē), 50 deva -
V/MRP/13/0001-06 10 ABPE flakons (kartona kastē), 5 deva -
V/MRP/13/0001-07 10 ABPE flakons (plastmasas kastē), 5 deva -
Mucosiffa - V/MRP/20/0011 Ceva Sante Animale,, Francija QI02AD02 cattle Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate and solvent for suspension for injection
International name (active substance): Live, attenuated Bovine Viral Diarrhoea type BVD-1virus, cytopath. strain Oregon C24
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Ceva-Phylaxia Veterinary Biologicals Co. Ltd., Ungārija
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 (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/MRP/20/0011-01 1 Stikla flakons, 1 deva -
V/MRP/20/0011-02 1 Stikla flakons, 2 deva -
V/MRP/20/0011-03 1 Stikla flakons, 5 deva -
V/MRP/20/0011-04 1 Stikla flakons, 10 deva -
V/MRP/20/0011-05 1 Stikla flakons, 20 deva -
V/MRP/20/0011-06 1 Stikla flakons, 50 deva -
Karallact 75 mg V/NRP/15/0005 Fatro S.p.A., Itālija QJ51DE90 cattle (lactating cows) Vairāk

Medicinal product information

Pharmaceutical form: intramammary ointment
International name (active substance): Cefquinome (as cefquinome sulfate)
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Fatro S.p.A., Itālija
Date of authorisation/renewal: 01-Oct-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Oct-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Oct-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (27-Oct-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/15/0005-01 75 mg 4 Polipropilēna pilnšļirce, 1 deva -
V/NRP/15/0005-02 75 mg 15 Polipropilēna pilnšļirce, 1 deva -
V/NRP/15/0005-03 75 mg 24 Polipropilēna pilnšļirce, 1 deva -
Ovulike 0.004 mg/ml V/MRP/17/0045 aniMedica GmbH, Vācija QH01CA90 cattle; horses; rabbits Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Buserelin acetate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release aniMedica GmbH, Vācija
Date of authorisation/renewal: 29-Mar-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_aprakst (27-Jul-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_aprakst (27-Jul-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (30-Dec-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/17/0045-01 5 Stikla flakons, 10 ml -
V/MRP/17/0045-02 50 Stikla flakons, 10 ml -
V/MRP/17/0045-03 100 Stikla flakons, 10 ml -
V/MRP/17/0045-04 250 Stikla flakons, 10 ml -
V/MRP/17/0045-05 500 Stikla flakons, 10 ml -
Advantix 100mg/500mg - V/NRP/25/0057 Elanco Animal Health GmbH, Vācija QP53AC54 dogs Vairāk

Medicinal product information

Pharmaceutical form: spot-on solution
International name (active substance): Imidacloprid, Permethrin
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release KVP Pharma + Veterinar Produkte GmbH, Vācija
Date of authorisation/renewal: 29-Dec-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (10-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/25/0057-01 1 Pipete, 1 ml -
V/NRP/25/0057-02 2 Pipete, 1 ml -
V/NRP/25/0057-03 3 Pipete, 1 ml -
V/NRP/25/0057-04 4 Pipete, 1 ml -
V/NRP/25/0057-05 6 Pipete, 1 ml -
Advantix 250mg/1250mg - V/NRP/25/0058 Elanco Animal Health GmbH, Vācija QP53AC54 dogs Vairāk

Medicinal product information

Pharmaceutical form: spot-on solution
International name (active substance): Imidacloprid, Permethrin
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release KVP Pharma + Veterinar Produkte GmbH, Vācija
Date of authorisation/renewal: 29-Dec-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (10-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/25/0058-01 1 Pipete, 2,5 ml -
V/NRP/25/0058-02 2 Pipete, 2,5 ml -
V/NRP/25/0058-03 3 Pipete, 2,5 ml -
V/NRP/25/0058-04 4 Pipete, 2,5 ml -
V/NRP/25/0058-05 6 Pipete, 2,5 ml -
Advantix 400mg/2000mg - V/NRP/25/0059 Elanco Animal Health GmbH, Vācija QP53AC54 dogs Vairāk

Medicinal product information

Pharmaceutical form: spot-on solution
International name (active substance): Imidacloprid, Permethrin
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release KVP Pharma + Veterinar Produkte GmbH, Vācija
Date of authorisation/renewal: 29-Dec-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (10-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (10-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/25/0059-01 1 Pipete, 4 ml -
V/NRP/25/0059-02 2 Pipete, 4 ml -
V/NRP/25/0059-03 3 Pipete, 4 ml -
V/NRP/25/0059-04 4 Pipete, 4 ml -
V/NRP/25/0059-05 6 Pipete, 4 ml -
Moxisolv LA 100 mg/ml V/DCP/23/0006 Bimeda Animal Health Limited, Īrija QP54AB02 cattle Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Moxidectin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bimeda Animal Health Limited, Īrija
Date of authorisation/renewal: 23-Feb-2023
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
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/DCP/23/0006-01 100 mg/ml 1 ABPE pudele, 50 ml -
V/DCP/23/0006-02 100 mg/ml 1 ABPE pudele, 200 ml -
Micospectone - V/NRP/01/1379 Fatro S.p.A., Itālija QJ01FF52 cattle; pigs; sheep; goats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Lincomycin hydrohloride, Spectinomycin hydrochloride
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 (03-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (03-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (03-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/01/1379-01 1 Stikla flakons, 50 ml -
V/NRP/01/1379-02 1 Stikla flakons, 100 ml -
V/NRP/01/1379-03 1 Stikla flakons, 250 ml -
V/NRP/01/1379-04 1 Stikla flakons, 500 ml -
Milpro 4 mg/10 mg - V/MRP/20/0025 VIRBAC, Francija QP54AB51 small cats

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 VIRBAC, Francija
Date of authorisation/renewal: 28-Jan-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_aprakst (22-Aug-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (22-Aug-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (22-Aug-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/20/0025-01 4 mg/10 mg 1 Al/Al blisteris, 2 tablete -
V/MRP/20/0025-02 4 mg/10 mg 2 Al/Al blisteris, 2 tablete -
V/MRP/20/0025-03 4 mg/10 mg 12 Al/Al blisteris, 2 tablete -
Milpro 16 mg/40 mg - V/MRP/20/0026 VIRBAC, Francija QP54AB51 cats 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 VIRBAC, Francija
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 (22-Aug-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (22-Aug-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (22-Aug-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/20/0026-01 16 mg/40 mg 1 Al/Al blisteris, 2 tablete -
V/MRP/20/0026-02 16 mg/40 mg 2 Al/Al blisteris, 2 tablete -
V/MRP/20/0026-03 16 mg/40 mg 12 Al/Al blisteris, 2 tablete -
V/MRP/20/0026-04 16 mg/40 mg 24 Al/Al blisteris, 2 tablete -
Milpro 2,5 mg/ 25 mg - V/MRP/20/0027 VIRBAC, Francija QP54AB51 small dogs; puppies 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 VIRBAC, Francija
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 (24-Feb-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (24-Feb-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (24-Oct-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/20/0027-01 2,5 mg/25 mg 1 Al/Al blisteris, 2 tablete -
V/MRP/20/0027-02 2,5 mg/25 mg 2 Al/Al blisteris, 2 tablete -
V/MRP/20/0027-03 2,5 mg/25 mg 12 Al/Al blisteris, 2 tablete -
Fatroximin 300/4 mg/g - V/NRP/01/1369 Fatro S.p.A., Itālija QG51AA06 cattle; horses Vairāk

Medicinal product information

Pharmaceutical form: pessary
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 (11-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (11-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (11-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/01/1369-01 300 mg/pesārijs 12 Blisteris, 1 pesārijs -
V/NRP/01/1369-02 300 mg/pesārijs 36 Blisteris, 1 pesārijs -
Fatroximin 100/13.4 mg/g - V/NRP/01/1371 Fatro S.p.A., Itālija QG51AA06 mares; cows Vairāk

Medicinal product information

Pharmaceutical form: intrauterine foam
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 (04-Nov-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (04-Nov-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (04-Nov-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/01/1371-01 100 mg/deva 6 Alumīnija balons, 1 deva -

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