Veterinary medicinal product register

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Data selected by 705
Original name Strength Marketing authorisation number Marketing authorisation holder: ATCvet code Species More
Carprodolor 50 mg/ml V/DCP/13/0011 Le Vet Beheer B.V., Nīderlande 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 Produlab Pharma b.v., Nīderlande
Date of authorisation/renewal: 09-Oct-2018
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] 28092018LI (28-Nov-2023)
Labelling text: [PDF] 28092018M (28-Nov-2023)
Summary of product characteristics: [DOCX] 28092018ZA (28-Nov-2023)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/13/0011-01 50 mg/ml 1 Stikla pudele (dzintarkrāsas), 50 ml [PDF] [PDF]
Forthyron flavour 200 µg/tabl. V/MRP/18/0049 Eurovet Animal Health B.V., Nīderlande QH03AA01 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Levothyroxine sodium
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Eurovet Animal Health B.V., Nīderlande;Dales Pharmaceuticals Ltd., Lielbritānija;Genera d.d., Horvātija
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 (17-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (17-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/18/0049-01 50 alumīnija/PVC/PE/PVDC blisteris, 10 tablete -
V/MRP/18/0049-02 250 alumīnija/PVC/PE/PVDC blisteris, 10 tablete -
Forthyron flavour 400 µg/tabl. V/MRP/18/0050 Eurovet Animal Health B.V., Nīderlande QH03AA01 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Levothyroxine sodium
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Eurovet Animal Health B.V., Nīderlande;Dales Pharmaceuticals Ltd., Lielbritānija;Genera d.d., Horvātija
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 (17-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (17-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/18/0050-01 50 alumīnija/PVC/PE/PVDC blisteris, 10 tablete -
V/MRP/18/0050-02 250 alumīnija/PVC/PE/PVDC blisteris, 10 tablete -
Forthyron flavour 600 µg/tabl. V/MRP/18/0051 Eurovet Animal Health B.V., Nīderlande QH03AA01 dogs Vairāk

Medicinal product information

Pharmaceutical form: tablets
International name (active substance): Levothyroxine sodium
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Eurovet Animal Health B.V., Nīderlande;Dales Pharmaceuticals Ltd., Lielbritānija;Genera d.d., Horvātija
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 (17-Sep-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (17-Sep-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (17-Sep-2025)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/18/0051-01 50 alumīnija/PVC/PE/PVDC blisteris, 10 tablete -
V/MRP/18/0051-02 250 alumīnija/PVC/PE/PVDC blisteris, 10 tablete -
Amphen 200 mg/g V/DCP/20/0004 Huvepharma NV, Beļģija QJ01BA90 pigs Vairāk

Medicinal product information

Pharmaceutical form: granules for use in drinking water
International name (active substance): Florfenicol
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Laboratoria Smeets NV, 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 (28-Jan-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (28-Jan-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (28-Jan-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/20/0004-01 200 mg/g 1 Maiss, 0,5 kg -
V/DCP/20/0004-02 200 mg/g 1 Maiss, 1 kg -
Pronestesic - V/DCP/16/0009 Fatro S.p.A., Itālija QN01BA52 cattle; pigs; sheep; horses Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Procaine hydrochloride, Epinephrine tartrate
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release Fatro S.p.A., Itālija
Date of authorisation/renewal: 21-May-2021
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Feb-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Feb-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (27-Feb-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/16/0009-01 1 Stikla pudelīte (dzintarkrāsas), 50 ml -
V/DCP/16/0009-02 1 Stikla pudelīte (dzintarkrāsas), 100 ml -
V/DCP/16/0009-03 1 Stikla pudelīte (dzintarkrāsas), 250 ml -
V/DCP/16/0009-04 10 Stikla pudelīte (dzintarkrāsas), 100 ml -
Orbeseal 2.6 g V/NRP/03/1565 Zoetis Belgium S.A., Beļģija QG52X cattle Vairāk

Medicinal product information

Pharmaceutical form: intramammary suspension
International name (active substance): Bismuth subnitrate
Distribution category: Nonprescription veterinary medicinal product
Manufacturer(s) responsible for batch release Cross Vetpharm Group Ltd. T/A Bimeda, Īrija;Haupt Pharma Latina s.r.l., Itālija
Date of authorisation/renewal: 15-Jul-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (23-Jan-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (23-Jan-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (23-Jan-2023)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/03/1565-01 2,6 g/deva 24 Injektors, 1 deva -
V/NRP/03/1565-02 2,6 g/deva 60 Injektors, 1 deva -
V/NRP/03/1565-03 2,6 g/deva 120 Injektors, 1 deva -
Temprace Vet 0.5 mg/ml V/DCP/18/0015 Le Vet Beheer B.V., Nīderlande QN05AA04 dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Acepromazin
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release Produlab Pharma b.v., 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 (25-Mar-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (25-Mar-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (25-Mar-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/18/0015-01 1 Stikla flakons, 10 ml -
V/DCP/18/0015-02 1 Stikla flakons, 20 ml -
V/DCP/18/0015-03 1 Stikla flakons, 100 ml -
Tranquinervin Vet 10 mg/ml V/DCP/18/0016 Le Vet Beheer B.V., Nīderlande QN05AA04 horses Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Acepromazin
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release Produlab Pharma b.v., 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 (25-Mar-2025)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (25-Mar-2025)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (25-Mar-2025)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/18/0016-01 1 Stikla flakons, 10 ml -
V/DCP/18/0016-02 1 Stikla flakons, 20 ml -
V/DCP/18/0016-03 1 Stikla flakons, 100 ml -
Uniferon 200 mg/ml V/MRP/10/0035 Pharmacosmos A/S, Dānija QB03AC pigs Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Complex of iron hydroxide
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Pharmacosmos A/S, Dānija
Date of authorisation/renewal: 29-Dec-2015
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [DOCX] 080524LI (08-May-2024)
Labelling text: [DOCX] 080524M (08-May-2024)
Summary of product characteristics: [DOCX] 080524ZA (08-May-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/10/0035-01 200 mg/ml 5 ABPE pudelīte, 100 ml -
V/MRP/10/0035-02 200 mg/ml 12 ABPE pudelīte, 100 ml -
V/MRP/10/0035-03 200 mg/ml 20 ABPE pudelīte, 100 ml -
V/MRP/10/0035-04 200 mg/ml 5 ZBPE pudelīte alumīnija folijā, 100 ml -
V/MRP/10/0035-05 200 mg/ml 12 ZBPE pudelīte alumīnija folijā, 100 ml -
V/MRP/10/0035-06 200 mg/ml 20 ZBPE pudelīte alumīnija folijā, 100 ml -
V/MRP/10/0035-07 200 mg/ml 12 ZBPE pudelīte alumīnija folijā, 200 ml -
V/MRP/10/0035-08 200 mg/ml 5 Stikla pudelīte, 100 ml -
V/MRP/10/0035-09 200 mg/ml 12 Stikla pudelīte, 100 ml -
V/MRP/10/0035-10 200 mg/ml 20 Stikla pudelīte, 100 ml -
V/MRP/10/0035-11 200 mg/ml 12 ZBPE pudelīte caurspīdīgā folijā, 200 ml -
V/MRP/10/0035-12 200 mg/ml 5 ZBPE pudelīte caurspīdīgā folijā, 100 ml -
V/MRP/10/0035-13 200 mg/ml 12 ZBPE pudelīte caurspīdīgā folijā, 100 ml -
V/MRP/10/0035-14 200 mg/ml 20 ZBPE pudelīte caurspīdīgā folijā, 100 ml -
INTRAMAR SEAL 2.6 g V/MRP/23/0037 Bioveta a.s., Čehija QG52X cattle Vairāk

Medicinal product information

Pharmaceutical form: intramammary suspension
International name (active substance): Bismuth subnitrate
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Bioveta, a.s., Čehija
Date of authorisation/renewal: 27-Jul-2023
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: MRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Jul-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (27-Jul-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (10-Sep-2024)

Products

ID Strength Package size Primary packaging Labelling
V/MRP/23/0037-01 24 Injektors, 4 g -
V/MRP/23/0037-02 160 Injektors, 4 g -
Selehold 15 mg V/DCP/18/0065 KRKA, d.d., Novo mesto, Slovēnija QP54AA05 cats ≤ 2,5 kg; dogs ≤ 2,5 kg Vairāk

Medicinal product information

Pharmaceutical form: spot-on solution
International name (active substance): Selamectin
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: 04-Dec-2018
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Dec-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Dec-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (20-Dec-2023)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/18/0065-01 1 Polipropilēna pipete, 0,25 ml/deva -
V/DCP/18/0065-02 3 Polipropilēna pipete, 0,25 ml/deva -
V/DCP/18/0065-03 6 Polipropilēna pipete, 0,25 ml/deva -
V/DCP/18/0065-04 15 Polipropilēna pipete, 0,25 ml/deva -
Selehold 60 mg V/DCP/18/0067 KRKA, d.d., Novo mesto, Slovēnija QP54AA05 cats 7,6 - 10,0 kg Vairāk

Medicinal product information

Pharmaceutical form: spot-on solution
International name (active substance): Selamectin
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: 04-Dec-2018
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Dec-2023)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (20-Dec-2023)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (20-Dec-2023)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/18/0067-01 1 Polipropilēna pipete, 1 ml/deva -
V/DCP/18/0067-02 3 Polipropilēna pipete, 1 ml/deva -
V/DCP/18/0067-03 6 Polipropilēna pipete, 1 ml/deva -
V/DCP/18/0067-04 15 Polipropilēna pipete, 1 ml/deva -
Progressis - V/NRP/03/1542 Ceva Sante Animale', Francija QI09AA05 pigs Vairāk

Medicinal product information

Pharmaceutical form: emulsion for injection
International name (active substance): Inactivated porcine reproductive and respiratory syndrome virus, strain P120
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: 18-Aug-2008
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: NRP
Package leaflet: [PDF] Skat_sadaļā_Zāļu_apraksts (05-Nov-2024)
Labelling text: [PDF] Skat_sadaļā_Zāļu_apraksts (05-Nov-2024)
Summary of product characteristics: [DOCX] Zāļu_informācija_ZA_M_LI (11-Jul-2025)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/03/1542-01 10 Flakons, 1 deva -
V/NRP/03/1542-02 25 Flakons, 1 deva -
V/NRP/03/1542-03 1 Flakons, 5 deva -
V/NRP/03/1542-04 10 Flakons, 5 deva -
V/NRP/03/1542-05 1 Flakons, 10 deva -
V/NRP/03/1542-06 10 Flakons, 10 deva -
V/NRP/03/1542-07 1 Flakons, 25 deva -
V/NRP/03/1542-08 10 Flakons, 25 deva -
V/NRP/03/1542-09 1 ZBPE flakons, 50 deva -
V/NRP/03/1542-10 10 ZBPE flakons, 50 deva -
Alfatrim 24% - V/NRP/97/0540 Alfasan International B.V., Nīderlande QJ01EW30 cattle; pigs; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Trimethoprim, Sulfametoxasole
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: [PDF] 200218LI (05-Mar-2018)
Labelling text: [PDF] 200218M (05-Mar-2018)
Summary of product characteristics: [DOCX] 27102021ZA (27-Oct-2021)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/97/0540-01 1 Flakons, 100 ml -
V/NRP/97/0540-02 12 Flakons, 100 ml -
BI-VAC 2 - V/NRP/02/1500 Fatro S.p.A., Itālija QI01AD07 poultry Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate for oral solution
International name (active substance): Live attenuated Infectious Bronchitis virus
Distribution category: To be used only by veterinary surgeon
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] 89-130608LI (13-Jun-2008)
Labelling text: [PDF] 89-130608M (13-Jun-2008)
Summary of product characteristics: [PDF] 89-130608ZA (13-Jun-2008)

Products

ID Strength Package size Primary packaging Labelling
V/NRP/02/1500-01 1 Stikla flakons, 1000 deva -
V/NRP/02/1500-02 10 Stikla flakons, 1000 deva -
Cevac Meta L - V/DCP/16/0029 Ceva-Phylaxia Veterinary Biologicals Co. Ltd., Ungārija QI01AD01 chickens Vairāk

Medicinal product information

Pharmaceutical form: lyophilisate for oculonasal suspension
International name (active substance): Live, attenuated avian metapneumovirus subtype B, strain CRR126
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: 29-Nov-2021
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 26112021LI (26-Nov-2021)
Labelling text: [DOCX] 26112021M (26-Nov-2021)
Summary of product characteristics: [DOCX] 26112021ZA (26-Nov-2021)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/16/0029-01 1 Stikla flakons, 500 deva -
V/DCP/16/0029-02 1 Stikla flakons, 1000 deva -
V/DCP/16/0029-03 1 Stikla flakons, 2000 deva -
V/DCP/16/0029-04 1 Stikla flakons, 2500 deva -
V/DCP/16/0029-05 1 Stikla flakons, 3000 deva -
V/DCP/16/0029-06 1 Stikla flakons, 4000 deva -
V/DCP/16/0029-07 1 Stikla flakons, 5000 deva -
V/DCP/16/0029-08 10 Stikla flakons, 500 deva -
V/DCP/16/0029-09 10 Stikla flakons, 1000 deva -
V/DCP/16/0029-10 10 Stikla flakons, 2000 deva -
V/DCP/16/0029-11 10 Stikla flakons, 2500 deva -
V/DCP/16/0029-12 10 Stikla flakons, 3000 deva -
V/DCP/16/0029-13 10 Stikla flakons, 4000 deva -
V/DCP/16/0029-14 10 Stikla flakons, 5000 deva -
V/DCP/16/0029-15 20 Stikla flakons, 500 deva -
V/DCP/16/0029-16 20 Stikla flakons, 1000 deva -
V/DCP/16/0029-17 20 Stikla flakons, 2000 deva -
V/DCP/16/0029-18 20 Stikla flakons, 2500 deva -
V/DCP/16/0029-19 20 Stikla flakons, 3000 deva -
V/DCP/16/0029-20 20 Stikla flakons, 4000 deva -
Aniketam 100 mg/ml V/DCP/14/0042 Le Vet Beheer B.V., Nīderlande QN01AX03 guinea pigs; hamsters; cattle; pigs; sheep; goats; horses; mouses; rats; dogs; cats; rabbits Vairāk

Medicinal product information

Pharmaceutical form: solution for injection
International name (active substance): Ketamine hydrochloride
Distribution category: To be used only by veterinary surgeon
Manufacturer(s) responsible for batch release Produlab Pharma b.v., Nīderlande
Date of authorisation/renewal: 03-Jul-2019
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [PDF] 040719LI (04-Jul-2019)
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/14/0042-01 100 mg/ml 1 Stikla pudelīte (dzintarkrāsas), 10 ml -
V/DCP/14/0042-02 100 mg/ml 1 Stikla pudelīte (dzintarkrāsas), 25 ml -
V/DCP/14/0042-03 100 mg/ml 1 Stikla pudelīte (dzintarkrāsas), 50 ml -
Dophalin 400 mg/g V/DCP/17/0030 VETPHARMA ANIMAL HEALTH, S.L, Spānija QJ01FF02 pigs; chickens Vairāk

Medicinal product information

Pharmaceutical form: Powder for use in drinking water
International name (active substance): Lincomycin
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release MEVET S.A.U, Spānija;PROVET A.E, Grieķija
Date of authorisation/renewal: 28-Jun-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
Package leaflet: [DOCX] 07052025LI (07-May-2025)
Labelling text: [DOCX] 07052025M (07-May-2025)
Summary of product characteristics: [DOCX] 16062024ZA (16-Jun-2024)

Products

ID Strength Package size Primary packaging Labelling
V/DCP/17/0030-01 400 mg/g 1 Polipropilēna maiss, 1 kg -
V/DCP/17/0030-02 400 mg/g 1 Polipropilēna maiss, 150 g -
Ophtaclin vet 10 mg/g V/DCP/17/0034 Le Vet Beheer B.V., Nīderlande QS01AA02 horses; dogs; cats Vairāk

Medicinal product information

Pharmaceutical form: eye ointment
International name (active substance): Chlortetracycline hydrochloride
Distribution category: To be supplied only on veterinary prescription
Manufacturer(s) responsible for batch release Produlab Pharma b.v., Nīderlande
Date of authorisation/renewal: 27-Sep-2022
Marketing authorisation valid until: Unlimited time period
Marketing authorisation procedure: DCP
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/DCP/17/0034-01 1 Alumīnija tūbiņa, 5 g -

3081 record

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