|
Varostop
|
3.6 mg
|
V/NRP/14/0007
|
Bičiu Austeja, Lietuva
|
QP53AC05
|
honey bees
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
bee-hive strip
|
| International name (active substance): |
Flumethrin
|
| Distribution category: |
Nonprescription veterinary medicinal product
|
| Manufacturer(s) responsible for batch release |
Primavet - Sofija Ltd, Bulgārija
|
| Date of authorisation/renewal: |
04-Dec-2018
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[PDF] 301118LI (30-Nov-2018)
|
| Labelling text: |
[PDF] 301118M (30-Nov-2018)
|
| Summary of product characteristics: |
[PDF] 301118ZA (30-Nov-2018)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/14/0007-01 |
3,6 mg |
1 |
Alumīnija folijas maisiņš, 10 plāksnītes |
-
|
|
|
Ivocure
|
10 mg/ml
|
V/MRP/24/0072
|
Interchemie werken "De Adelaar" B.V., Nīderlande
|
QP54AA01
|
cattle; pigs; sheep
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/MRP/24/0072-01 |
|
1 |
Stikla flakons ar alumīnija vāciņu, 50 ml |
-
|
| V/MRP/24/0072-02 |
|
1 |
Stikla flakons ar alumīnija/plastmasas vāciņu, 50 ml |
-
|
|
|
PimoPET
|
5 mg
|
V/NRP/24/0073
|
Farma PET GIGI SIA, Latvija
|
QC01CE90
|
dogs
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/24/0073-01 |
|
1 |
ABPE konteiners, 30 tablete |
-
|
| V/NRP/24/0073-02 |
|
1 |
ABPE konteiners, 100 tablete |
-
|
|
|
Combi-kel 40
|
-
|
V/NRP/98/0716
|
Kela Laboratoria NV, Beļģija
|
QJ01RA01
|
cattle; pigs; sheep; goats; horses; 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 |
Kela Laboratoria NV, Beļģija
|
| Date of authorisation/renewal: |
18-Aug-2008
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[PDF] 220517LI (07-Jun-2017)
|
| Labelling text: |
[PDF] 220517M (07-Jun-2017)
|
| Summary of product characteristics: |
[PDF] 220517ZA (07-Jun-2017)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/98/0716-03 |
|
1 |
Stikla flakons, 100 ml |
-
|
|
|
Nobilis Salenvac T
|
-
|
V/NRP/05/1634
|
Intervet International B.V., Nīderlande
|
QI01AB01
|
chickens
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
suspension for injection
|
| International name (active substance): |
Killed cells of Salmonella enteritidis PT4,Killed cells of Salmonella typhimurium DT 104
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
Intervet International B.V., Nīderlande
|
| Date of authorisation/renewal: |
15-Feb-2010
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[PDF] Skat_sadaļā_Zāļu_apraksts (14-Aug-2025)
|
| Labelling text: |
[PDF] Skat_sadaļā_Zāļu_apraksts (14-Aug-2025)
|
| Summary of product characteristics: |
[DOCX] Zāļu_informācija_ZA_M_LI (14-Aug-2025)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/05/1634-02 |
|
1 |
Plastmasas pudele, 500 ml |
-
|
|
|
Dermipred
|
20 mg
|
V/MRP/18/0019
|
Ceva Sante Animale', Francija
|
QH02AB06
|
dogs
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/MRP/18/0019-01 |
|
2 |
AL/PVC-AL-PA blisteris, 10 tablete |
-
|
| V/MRP/18/0019-02 |
|
10 |
AL/PVC-AL-PA blisteris, 10 tablete |
-
|
| V/MRP/18/0019-03 |
|
2 |
AL/PVDC-TE-PVC blisteris, 10 tablete |
-
|
| V/MRP/18/0019-04 |
|
10 |
AL/PVDC-TE-PVC blisteris, 10 tablete |
-
|
|
|
Bolfo
|
4.442 g
|
V/NRP/09/0012
|
Elanco Animal Health GmbH, Vācija
|
QP53AE02
|
dogs
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/09/0012-01 |
4,442 g |
1 |
Poliestera/polietilēna/alumīnija maisiņš, 1 deva |
-
|
|
|
Bolfo
|
1.23 g
|
V/NRP/99/0982
|
Elanco Animal Health GmbH, Vācija
|
QP53AE02
|
dogs; cats
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/99/0982-01 |
1,23 g |
1 |
Poliestera/polietilēna/alumīnija maisiņš, 1 deva |
-
|
|
|
Morphasol
|
4 mg/ml
|
V/MRP/11/0070
|
aniMedica GmbH, Vācija
|
QN02AF01
|
dogs; cats
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/MRP/11/0070-01 |
4 mg/ml |
1 |
Stikla flakons, 10 ml |
-
|
| V/MRP/11/0070-03 |
4 mg/ml |
5 |
Stikla flakons, 10 ml |
-
|
|
|
Morphasol
|
10 mg/ml
|
V/MRP/11/0069
|
aniMedica GmbH, Vācija
|
QN02AF01
|
horses
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/MRP/11/0069-01 |
10 mg/ml |
1 |
Stikla flakons, 20 ml |
-
|
|
|
Dexamethasone 2 mg/ml
|
2 mg/ml
|
V/NRP/97/0602
|
Alfasan International B.V., Nīderlande
|
QH02AB02
|
cattle; pigs; sheep; goats; horses; 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 |
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] 210818LI (21-Aug-2018)
|
| Labelling text: |
[PDF] 210818M (21-Aug-2018)
|
| Summary of product characteristics: |
[PDF] 210818ZA (21-Aug-2018)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/97/0602-01 |
2 mg/ml |
1 |
Flakons, 100 ml |
-
|
| V/NRP/97/0602-02 |
2 mg/ml |
12 |
Flakons, 100 ml |
-
|
|
|
Tiamowet 200
|
162.2 mg/ml
|
V/NRP/00/1198
|
Vetoquinol Biowet Sp. z o.o., Polija
|
QJ01XQ01
|
pigs
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
solution for injection
|
| International name (active substance): |
Tiamulin
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
Vetoquinol Biowet Sp. z o.o., Polija
|
| Date of authorisation/renewal: |
13-May-2010
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[DOCX] 30122020LI (30-Dec-2020)
|
| Labelling text: |
[DOCX] 30122020M (10-Mar-2022)
|
| Summary of product characteristics: |
[DOCX] 30122020ZA (30-Dec-2020)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/00/1198-01 |
162,2 mg/ml |
1 |
Stikla (tumša) flakons, 100 ml |
-
|
|
|
Dalmarelin
|
25 µg/ml
|
V/NRP/01/1381
|
Fatro S.p.A., Itālija
|
QH01CA92
|
cattle; horses; rabbits
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/01/1381-01 |
25 µg/ml |
1 |
I tipa stikla flakons, 10 ml |
-
|
| V/NRP/01/1381-02 |
25 µg/ml |
1 |
Polietilēna maisiņš, 100 ml |
-
|
| V/NRP/01/1381-03 |
25 µg/ml |
1 |
II tipa stikla flakons, 10 ml |
-
|
| V/NRP/01/1381-04 |
25 µg/ml |
10 |
I tipa stikla flakons, 4 ml |
-
|
| V/NRP/01/1381-05 |
25 µg/ml |
1 |
II tipa stikla flakons, 20 ml |
-
|
| V/NRP/01/1381-06 |
25 µg/ml |
1 |
II tipa stikla flakons, 50 ml |
-
|
|
|
Fludosol
|
200 mg/ml
|
V/DCP/23/0005
|
Dopharma Research B.V., Nīderlande
|
QP52AC12
|
pigs; chickens
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/DCP/23/0005-01 |
200 mg/ml |
1 |
ABPE pudele, 250 ml |
-
|
| V/DCP/23/0005-03 |
200 mg/ml |
1 |
ABPE pudele, kas noslēgta ar ABPE skrūvējamu vāciņu, 1 l |
-
|
| V/DCP/23/0005-04 |
200 mg/ml |
1 |
ABPE pudele, kas noslēgta ar ZBPE skrūvējamu vāciņu, 1 l |
-
|
| V/DCP/23/0005-05 |
200 mg/ml |
1 |
Polietilēna kanna, 5 l |
-
|
|
|
Tirsan injection
|
250 mg/ml
|
V/NRP/01/1373
|
Fatro S.p.A., Itālija
|
QJ01BA02
|
cattle; pigs; sheep; piglets
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
solution for injection
|
| 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] 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/01/1373-01 |
250 mg/ml |
1 |
Stikla pudelīte, 40 ml |
-
|
| V/NRP/01/1373-02 |
250 mg/ml |
1 |
Stikla pudelīte, 100 ml |
-
|
| V/NRP/01/1373-03 |
250 mg/ml |
1 |
Stikla pudelīte, 250 ml |
-
|
| V/NRP/01/1373-04 |
250 mg/ml |
1 |
Stikla pudelīte, 500 ml |
-
|
|
|
Pyanosid Solution
|
-
|
V/NRP/96/0405
|
Bela-pharm GmbH&Co.KG, Vācija
|
QJ01FF52
|
cattle (calf); pigs; dogs; cats
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/96/0405-01 |
|
1 |
Stikla pudelīte, 50 ml |
-
|
| V/NRP/96/0405-02 |
|
6 |
Stikla pudelīte, 50 ml |
-
|
| V/NRP/96/0405-03 |
|
12 |
Stikla pudelīte, 50 ml |
-
|
| V/NRP/96/0405-08 |
|
1 |
Stikla pudelīte, 100 ml |
-
|
| V/NRP/96/0405-09 |
|
6 |
Stikla pudelīte, 100 ml |
-
|
| V/NRP/96/0405-10 |
|
12 |
Stikla pudelīte, 100 ml |
-
|
|
|
Helminthex
|
425.45 mg/g
|
V/DCP/19/0041
|
Bimeda Animal Health Limited., Īrija
|
QP52AF02
|
horses
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/DCP/19/0041-01 |
425,45 mg/g |
1 |
Šļirce, 27,5 g |
-
|
| V/DCP/19/0041-02 |
425,45 mg/g |
10 |
Šļirce, 27,5 g |
-
|
| V/DCP/19/0041-03 |
425,45 mg/g |
20 |
Šļirce, 27,5 g |
-
|
| V/DCP/19/0041-04 |
425,45 mg/g |
1 |
Šļirce, 32,08 g |
-
|
| V/DCP/19/0041-05 |
425,45 mg/g |
10 |
Šļirce, 32,08 g |
-
|
| V/DCP/19/0041-06 |
425,45 mg/g |
20 |
Šļirce, 32,08 g |
-
|
|
|
Recudon 2,5 mg/ml + 0,125 mg/ml
|
-
|
V/DCP/23/0047
|
Alfasan Nederland BV, Nīderlande
|
QN02AC52
|
horses; dogs
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/DCP/23/0047-01 |
|
1 |
Stikla flakons, 5 ml |
-
|
| V/DCP/23/0047-02 |
|
1 |
Stikla flakons, 10 ml |
-
|
| V/DCP/23/0047-03 |
|
1 |
Stikla flakons, 30 ml |
-
|
| V/DCP/23/0047-04 |
|
1 |
Stikla flakons, 50 ml |
-
|
|
|
Recudon 5 mg/ml + 0,25 mg/ml
|
-
|
V/DCP/23/0048
|
Alfasan Nederland BV, Nīderlande
|
QN02AC52
|
horses; dogs
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/DCP/23/0048-01 |
|
1 |
Stikla flakons, 5 ml |
-
|
| V/DCP/23/0048-02 |
|
1 |
Stikla flakons, 10 ml |
-
|
| V/DCP/23/0048-03 |
|
1 |
Stikla flakons, 30 ml |
-
|
| V/DCP/23/0048-04 |
|
1 |
Stikla flakons, 50 ml |
-
|
|
|
Cloxacillin-Benzathin
|
1000 mg
|
V/NRP/96/0399
|
AS Dimedium Latvija, Latvija
|
QJ51CF02
|
cattle
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
intramammary suspension
|
| International name (active substance): |
Cloxacillin benzathine
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
CP-Pharma Handelsgesellschaft GmbH, Vācija
|
| Date of authorisation/renewal: |
22-Sep-2008
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[DOCX] 01112022LI (01-Nov-2022)
|
| Labelling text: |
[DOCX] 01112022M (01-Nov-2022)
|
| Summary of product characteristics: |
[DOCX] 01112022ZA (01-Nov-2022)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/96/0399-01 |
|
4 |
Injektors, 1 deva |
-
|
| V/NRP/96/0399-02 |
|
80 |
Injektors, 1 deva |
-
|
| V/NRP/96/0399-03 |
|
20 |
Injektors, 1 deva |
-
|
|