|
Tirsan Powder
|
200 mg/g
|
V/NRP/01/1374
|
Fatro S.p.A., Itālija
|
QJ01BA02
|
pigs; broilers
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
oral powder
|
| International name (active substance): |
Thiamphenicol
|
| 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] 210717LI (30-Aug-2017)
|
| Labelling text: |
[PDF] 210717M (30-Aug-2017)
|
| Summary of product characteristics: |
[PDF] 210717ZA (30-Aug-2017)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/01/1374-01 |
200 mg/g |
1 |
Papīra maisiņš, 10 kg |
-
|
| V/NRP/01/1374-02 |
200 mg/g |
1 |
Papīra maiss, 25 kg |
-
|
|
|
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
|
|
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
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
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
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
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
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
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
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
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 |
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