|
Neostomosan concentrate
|
-
|
V/NRP/97/0510
|
Ceva Sante Animale', Francija
|
QP53AC13
|
horses; dogs; cats
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/97/0510-01 |
|
5 |
Ampula, 5 ml |
-
|
| V/NRP/97/0510-02 |
|
100 |
Ampula, 5 ml |
-
|
| V/NRP/97/0510-03 |
|
1 |
Pudele, 200 ml |
-
|
| V/NRP/97/0510-04 |
|
1 |
Pudele, 1 l |
-
|
| V/NRP/97/0510-05 |
|
1 |
Pudele, 5 l |
-
|
| V/NRP/97/0510-06 |
|
1 |
Pudele, 250 ml |
-
|
|
|
Galastop
|
50 µg/ml
|
V/NRP/03/1618
|
Ceva Sante Animale', Francija
|
QG02CB03
|
dogs
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/03/1618-01 |
50 µg/ml |
1 |
Flakons, 3 ml |
-
|
| V/NRP/03/1618-02 |
50 µg/ml |
1 |
Flakons, 7 ml |
-
|
| V/NRP/03/1618-03 |
50 µg/ml |
1 |
Flakons, 15 ml |
-
|
|
|
Cestal Plus
|
-
|
V/NRP/17/0009
|
Ceva Sante Animale', Francija
|
QP52AA51
|
dogs
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/17/0009-01 |
|
1 |
Alumīnija blisteris, 2 tablete |
-
|
| V/NRP/17/0009-02 |
|
2 |
Alumīnija blisteris, 2 tablete |
-
|
| V/NRP/17/0009-03 |
|
52 |
Alumīnija blisteris, 2 tablete |
-
|
| V/NRP/17/0009-04 |
|
1 |
Alumīnija blisteris, 8 tablete |
-
|
| V/NRP/17/0009-05 |
|
13 |
Alumīnija blisteris, 8 tablete |
-
|
| V/NRP/17/0009-06 |
|
25 |
Alumīnija blisteris, 8 tablete |
-
|
| V/NRP/17/0009-07 |
|
5 |
Polietilēna sloksnīte, 2 tablete |
-
|
| V/NRP/17/0009-08 |
|
100 |
Polietilēna sloksnīte, 2 tablete |
-
|
|
|
Zuritol
|
50 mg/ml
|
V/DCP/13/0051
|
Laboratorios Calier, S.A., Spānija
|
QP51BC01
|
pigs
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/DCP/13/0051-01 |
50 mg/ml |
1 |
ABPE pudele, 250 ml |
-
|
| V/DCP/13/0051-02 |
50 mg/ml |
1 |
ABPE pudele, 1000 ml |
-
|
|
|
Parofor crypto
|
140000 IU/ml
|
V/MRP/19/0047
|
Huvepharma NV, Beļģija
|
QA07AA06
|
pre-ruminant cattle
|
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/MRP/19/0047-01 |
140000 IU/ml |
1 |
ABPE pudele, 125 ml |
-
|
| V/MRP/19/0047-02 |
140000 IU/ml |
1 |
ABPE pudele, 250 ml |
-
|
| V/MRP/19/0047-03 |
140000 IU/ml |
1 |
ABPE pudele, 500 ml |
-
|
| V/MRP/19/0047-04 |
140000 IU/ml |
1 |
ABPE pudele, 1 l |
-
|
|
|
Vetoryl
|
60 mg
|
V/SRP/25/0027
|
Dechra Regulatory B.V., Nīderlande
|
QH02CA01
|
dogs
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/SRP/25/0027-01 |
|
1 |
PA/Al/PVH blisteris, 10 tablete |
-
|
| V/SRP/25/0027-02 |
|
3 |
PA/Al/PVH blisteris, 10 tablete |
-
|
| V/SRP/25/0027-03 |
|
5 |
PA/Al/PVH blisteris, 10 tablete |
-
|
| V/SRP/25/0027-04 |
|
6 |
PA/Al/PVH blisteris, 10 tablete |
-
|
| V/SRP/25/0027-05 |
|
10 |
PA/Al/PVH blisteris, 10 tablete |
-
|
|
|
Alzane
|
5 mg/ml
|
V/MRP/11/0045
|
LABORATORIOS SYVA S.A., Spānija
|
QV03AB90
|
dogs; cats
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/MRP/11/0045-01 |
5 mg/ml |
1 |
Stikla flakons, 10 ml |
[JPG]
[JPG]
[PDF]
|
| V/MRP/11/0045-02 |
5 mg/ml |
5 |
Stikla flakons, 10 ml |
[PDF]
|
| V/MRP/11/0045-03 |
5 mg/ml |
10 |
Stikla flakons, 10 ml |
[PDF]
|
|
|
Alphaflorovet
|
20 mg/g
|
V/DCP/19/0056
|
Alphavet Zrt., Ungārija
|
QJ01BA90
|
pigs
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
premix for medicated feeding stuff
|
| International name (active substance): |
Florfenicol
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
Alphavet Zrt., Ungārija
|
| Date of authorisation/renewal: |
28-Jan-2022
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
DCP
|
| Package leaflet: |
[DOCX] 23062025LIM (23-Jun-2025)
|
| Labelling text: |
[DOCX] 23062025LIM (23-Jun-2025)
|
| Summary of product characteristics: |
[DOCX] 23062025ZA (23-Jun-2025)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/DCP/19/0056-01 |
20 mg |
1 |
Trīs slāņu papīra maiss ar polietilēna iekšējo slāni , 10 kg |
-
|
|
|
Coglapix
|
-
|
V/MRP/15/0041
|
Ceva-Phylaxia Veterinary Biologicals Co. Ltd., Ungārija
|
QI09AB07
|
pigs
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
suspension for injection
|
| International name (active substance): |
Actinobacillus pleuropneumoniae serotype 1, strain NT3, Actinobacillus pleuropneumoniae serotype 2 (strains PO, U3, B4, SZ II)
|
| 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: |
08-Jan-2020
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
MRP
|
| Package leaflet: |
[PDF] Skat_sadaļā_Zāļu_apraksts (18-Feb-2025)
|
| Labelling text: |
[PDF] Skat_sadaļā_Zāļu_apraksts (18-Feb-2025)
|
| Summary of product characteristics: |
[DOCX] Zāļu_informācija_ZA_M_LI (11-Apr-2025)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/MRP/15/0041-01 |
|
1 |
Flakons, 50 deva |
-
|
| V/MRP/15/0041-02 |
|
5 |
Flakons, 50 deva |
-
|
|
|
Alphadoxan
|
100 mg/g
|
V/DCP/20/0039
|
Alphavet Zrt., Ungārija
|
QJ01AA02
|
pigs
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
premix for medicated feeding stuff
|
| International name (active substance): |
Doxycycline (as Doxycycline hyclate)
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
Alphavet Zrt, Ungārija
|
| Date of authorisation/renewal: |
28-Jan-2022
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
DCP
|
| Package leaflet: |
[DOCX] 02072025LIM (02-Jul-2025)
|
| Labelling text: |
[DOCX] 02072025LIM (02-Jul-2025)
|
| Summary of product characteristics: |
[DOCX] 02072025ZA (02-Jul-2025)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/DCP/20/0039-01 |
100 mg/g |
1 |
Trīs slāņu papīra maiss ar polietilēna iekšējo slāni , 10 kg |
-
|
|
|
Synthadon
|
5 mg/ml
|
V/DCP/14/0039
|
Le Vet Beheer B.V., Nīderlande
|
QN02AC90
|
dogs; cats
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/DCP/14/0039-01 |
5 mg/ml |
1 |
Stikla flakons, 5 ml |
-
|
| V/DCP/14/0039-02 |
5 mg/ml |
1 |
Stikla flakons, 10 ml |
-
|
| V/DCP/14/0039-03 |
5 mg/ml |
1 |
Stikla flakons, 20 ml |
-
|
| V/DCP/14/0039-04 |
5 mg/ml |
1 |
Stikla flakons, 25 ml |
-
|
| V/DCP/14/0039-05 |
5 mg/ml |
1 |
Stikla flakons, 30 ml |
-
|
| V/DCP/14/0039-06 |
5 mg/ml |
1 |
Stikla flakons, 50 ml |
-
|
|
|
Synthadon
|
10 mg/ml
|
V/DCP/14/0040
|
Le Vet Beheer B.V., Nīderlande
|
QN02AC90
|
dogs; cats
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/DCP/14/0040-01 |
10 mg/ml |
1 |
Stikla flakons, 5 ml |
-
|
| V/DCP/14/0040-02 |
10 mg/ml |
1 |
Stikla flakons, 10 ml |
-
|
| V/DCP/14/0040-03 |
10 mg/ml |
1 |
Stikla flakons, 20 ml |
-
|
| V/DCP/14/0040-04 |
10 mg/ml |
1 |
Stikla flakons, 25 ml |
-
|
| V/DCP/14/0040-05 |
10 mg/ml |
1 |
Stikla flakons, 30 ml |
-
|
| V/DCP/14/0040-06 |
10 mg/ml |
1 |
Stikla flakons, 50 ml |
-
|
|
|
Dophacyl Avi
|
1000 mg/g
|
V/DCP/24/0065
|
Dopharma Research B.V., Nīderlande
|
QN02BA04
|
chickens
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/DCP/24/0065-01 |
|
1 |
PP konteiners, 500 g |
-
|
| V/DCP/24/0065-02 |
|
1 |
PP konteiners, 1 kg |
-
|
| V/DCP/24/0065-03 |
|
1 |
Polipropilēna spainis, 1 kg |
-
|
| V/DCP/24/0065-04 |
|
1 |
Polipropilēna spainis, 2,5 kg |
-
|
| V/DCP/24/0065-05 |
|
1 |
Polipropilēna spainis, 5 kg |
-
|
| V/DCP/24/0065-06 |
|
1 |
Paciņa, 100 g |
-
|
|
|
Cadorex
|
300 mg/ml
|
V/MRP/17/0027
|
Industrial Veterinaria, S.A., Spānija
|
QJ01BA90
|
cattle; pigs; sheep
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/MRP/17/0027-01 |
300 mg/ml |
1 |
Polipropilēna pudelīte, 100 ml |
-
|
| V/MRP/17/0027-02 |
300 mg/ml |
1 |
Polipropilēna pudelīte, 250 ml |
-
|
|
|
Frontline Spot-on Cat
|
50 mg
|
V/NRP/98/0903
|
Boehringer Ingelheim Animal Health France SCS , Francija
|
QP53AX15
|
cats
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
solution for external use
|
| International name (active substance): |
Fipronil
|
| Distribution category: |
Nonprescription veterinary medicinal product
|
| Manufacturer(s) responsible for batch release |
Boehringer Ingelheim Animal Health France SCS., Francija
|
| Date of authorisation/renewal: |
15-Jul-2008
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[DOCX] 270623LI (27-Jun-2023)
|
| Labelling text: |
[DOCX] 270623M (27-Jun-2023)
|
| Summary of product characteristics: |
[DOCX] 270623ZA (27-Jun-2023)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/98/0903-01 |
50 mg/deva |
3 |
Pipete, 1 deva |
-
|
| V/NRP/98/0903-03 |
50 mg/deva |
1 |
Pipete, 1 deva |
-
|
|
|
Frontline Spot-on Dog S; M; L; XL
|
-
|
V/NRP/98/0902
|
Boehringer Ingelheim Animal Health France SCS , Francija
|
QP53AX15
|
dogs
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
solution for external use
|
| International name (active substance): |
Fipronil
|
| Distribution category: |
Nonprescription veterinary medicinal product
|
| Manufacturer(s) responsible for batch release |
Boehringer Ingelheim Animal Health France SCS., Francija
|
| Date of authorisation/renewal: |
15-Jul-2008
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[DOCX] 270623LI (27-Jun-2023)
|
| Labelling text: |
[DOCX] 270623M (27-Jun-2023)
|
| Summary of product characteristics: |
[DOCX] 270623ZA (27-Jun-2023)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/98/0902-01 |
100 mg/ml |
1 |
Pipete, 0,67 ml |
-
|
| V/NRP/98/0902-02 |
100 mg/ml |
1 |
Pipete, 1,34 ml |
-
|
| V/NRP/98/0902-03 |
100 mg/ml |
1 |
Pipete, 2,68 ml |
-
|
| V/NRP/98/0902-04 |
100 mg/ml |
1 |
Pipete, 4,02 ml |
-
|
| V/NRP/98/0902-05 |
100 mg/ml |
3 |
Pipete, 0,67 ml |
-
|
| V/NRP/98/0902-06 |
100 mg/ml |
3 |
Pipete, 1,34 ml |
-
|
| V/NRP/98/0902-07 |
100 mg/ml |
3 |
Pipete, 2,68 ml |
-
|
| V/NRP/98/0902-08 |
100 mg/ml |
3 |
Pipete, 4,02 ml |
-
|
|
|
Dormazolam
|
5 mg/ml
|
V/MRP/18/0047
|
Le Vet Beheer B.V., Nīderlande
|
QN05CD08
|
horses
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/MRP/18/0047-01 |
|
1 |
Stikla flakons, 5 ml |
-
|
| V/MRP/18/0047-02 |
|
1 |
Stikla flakons, 10 ml |
-
|
| V/MRP/18/0047-03 |
|
1 |
Stikla flakons, 20 ml |
-
|
| V/MRP/18/0047-04 |
|
1 |
Stikla flakons, 50 ml |
-
|
|
|
Pharmasin 500 WSP
|
500 mg/g
|
V/NRP/08/1714
|
Huvepharma NV, Beļģija
|
QJ01FA90
|
cattle (calf); pigs; turkeys; chickens
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/08/1714-01 |
500 mg/g |
1 |
Polipropilēna pudelīte, 100 g |
-
|
| V/NRP/08/1714-02 |
500 mg/g |
1 |
Polipropilēna pudelīte, 200 g |
-
|
| V/NRP/08/1714-04 |
500 mg/g |
1 |
Maisiņš, 1 kg |
-
|
| V/NRP/08/1714-06 |
500 mg/ml |
1 |
Maisiņš, 25 kg |
-
|
|
|
OTIBIOVIN
|
-
|
V/NRP/97/0579
|
Bioveta, a.s., Čehija
|
QS03C
|
dogs; cats
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
ear drops, solution
|
| International name (active substance): |
Salicylic acid,Carbethopendecinium bromatum,Gentamicin sulphate,Triamcinolone acetonide
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
Bioveta, a.s., Čehija
|
| Date of authorisation/renewal: |
05-Jul-2012
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[PDF] 290612LI (05-Jul-2012)
|
| Labelling text: |
[PDF] 290612M (05-Jul-2012)
|
| Summary of product characteristics: |
[PDF] 290612ZA (05-Jul-2012)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/97/0579-01 |
|
1 |
Polietilēna flakons, 15 ml |
-
|
| V/NRP/97/0579-02 |
|
1 |
Polietilēna flakons, 20 ml |
-
|
|
|
Lysvulpen por.
|
-
|
V/NRP/97/0592
|
Bioveta, a.s., Čehija
|
QI07BD
|
raccoon dogs; foxes
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
suspension for oral use
|
| International name (active substance): |
Attenuated live rabies virus
|
| Distribution category: |
To be used only by veterinary surgeon
|
| Manufacturer(s) responsible for batch release |
Bioveta, a.s., Čehija
|
| Date of authorisation/renewal: |
19-Jan-2012
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[PDF] 290716LI (02-Aug-2016)
|
| Labelling text: |
[PDF] 09032020M (09-Mar-2020)
|
| Summary of product characteristics: |
[PDF] 290716ZA (02-Aug-2016)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/97/0592-01 |
|
30 |
Kartona kastīte, 20 deva |
-
|
| V/NRP/97/0592-02 |
|
1 |
Polietilēna maiss, 350 deva |
-
|
| V/NRP/97/0592-03 |
|
1 |
Polietilēna maiss, 400 deva |
-
|
| V/NRP/97/0592-04 |
|
1 |
Poliolefīna maiss, 500 deva |
-
|
| V/NRP/97/0592-05 |
|
1 |
Polietilēna maiss, 600 deva |
-
|
| V/NRP/97/0592-06 |
|
1 |
Polietilēna maiss, 700 deva |
-
|
| V/NRP/97/0592-07 |
|
1 |
Polietilēna maiss, 800 deva |
-
|
| V/NRP/97/0592-08 |
|
1 |
Polietilēna maiss, 900 deva |
-
|
| V/NRP/97/0592-09 |
|
1 |
Poliolefīna maiss, 1000 deva |
-
|
| V/NRP/97/0592-10 |
|
10 |
Kartona kastīte, 40 deva |
-
|
|