|
Tetra-Bol
|
2000 mg
|
V/NRP/95/0150
|
AS Dimedium Latvija, Latvija
|
QG51AA02
|
cattle
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
intra-uterine tablets
|
| International name (active substance): |
Tetracycline hydrochloridum
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
CP-Pharma Handelsgesellschaft GmbH, Vācija
|
| Date of authorisation/renewal: |
15-Jul-2008
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[DOCX] 18122020LI (18-Dec-2020)
|
| Labelling text: |
[DOCX] 18122020M (18-Dec-2020)
|
| Summary of product characteristics: |
[DOCX] 18122020ZA (18-Dec-2020)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/95/0150-01 |
2000 mg |
20 |
Blisteris, 5 tablete |
-
|
| V/NRP/95/0150-02 |
2000 mg |
1 |
PE maisiņš, 100 tablete |
-
|
|
|
Vitamin E - Selen - Lösung
|
-
|
V/NRP/95/0258
|
AS Dimedium Latvija, Latvija
|
QA12CE99
|
cattle; pigs; sheep; goats
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
solution for injection
|
| International name (active substance): |
Vitamin E-acetate,Sodium selenite
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
CP-Pharma Handelsgesellschaft GmbH, Vācija
|
| Date of authorisation/renewal: |
07-Dec-2012
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[DOCX] 18122020LI (18-Dec-2020)
|
| Labelling text: |
[DOCX] 18122020M (18-Dec-2020)
|
| Summary of product characteristics: |
[DOCX] 18122020ZA (18-Dec-2020)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/95/0258-01 |
|
1 |
Stikla flakons, 100 ml |
-
|
|
|
Eurofit gel a.u.v.
|
-
|
V/NRP/11/0058
|
AS Dimedium Latvija, Latvija
|
QV03AX
|
cattle
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
gel
|
| International name (active substance): |
Arnica montana,Nitric acid,Horsefly weed,Bryonia,Narrow-leaved coneflower,Hepar sulfuris,Iodine,Pulsatilla,Phosphor,Sepia officinalis,Silicea,Poke root,Thuja occidentalis,Calcarea phosphorica,Cantharis vesicatoria,Phellandrium aquaticum
|
| Distribution category: |
Nonprescription veterinary medicinal product
|
| Manufacturer(s) responsible for batch release |
Slovenska zooveterinarna homeopaticka spolocnost, s.r.o., Slovākija
|
| Date of authorisation/renewal: |
29-Dec-2016
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[DOCX] 18122020LI (18-Dec-2020)
|
| Labelling text: |
[DOCX] 18122020M (18-Dec-2020)
|
| Summary of product characteristics: |
[DOCX] 18122020ZA (18-Dec-2020)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/11/0058-01 |
|
1 |
polietilēna šļirce, 30 ml |
-
|
|
|
Prosolvin
|
7.5 mg/ml
|
V/NRP/94/0093
|
Virbac S.A., Francija
|
QG02AD91
|
cattle; pigs; sheep; horses
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
solution for injection
|
| International name (active substance): |
Luprostiol
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
Virbac S.A., Francija
|
| Date of authorisation/renewal: |
30-Oct-2009
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[DOCX] 040820LI (04-Aug-2020)
|
| Labelling text: |
[DOCX] 040820M (04-Aug-2020)
|
| Summary of product characteristics: |
[DOCX] 040820ZA (04-Aug-2020)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/94/0093-01 |
7,5 mg/ml |
10 |
Flakons, 2 ml |
-
|
| V/NRP/94/0093-02 |
7,5 mg/ml |
1 |
Flakons, 10 ml |
-
|
| V/NRP/94/0093-03 |
7,5 mg/ml |
1 |
Flakons, 20 ml |
-
|
|
|
Enrobioflox 5%
|
50 mg/ml
|
V/NRP/00/1277
|
Vetoquinol Biowet Sp. z o.o., Polija
|
QJ01MA90
|
cattle; pigs; dogs
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
solution for injection
|
| International name (active substance): |
Enrofloxacin
|
| 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: |
27-Sep-2012
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[PDF] 210717LI (03-Nov-2017)
|
| Labelling text: |
[PDF] 210717M (03-Nov-2017)
|
| Summary of product characteristics: |
[PDF] 210717ZA (03-Nov-2017)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/00/1277-01 |
50 mg/ml |
1 |
Stikla (oranža) flakons, 50 ml |
-
|
| V/NRP/00/1277-02 |
50 mg/ml |
1 |
Stikla (oranža) flakons, 100 ml |
-
|
|
|
Tetanusan 24%
|
-
|
V/NRP/09/0005
|
Kon-Pharma GmbH, Vācija
|
QB05XA30
|
cattle; pigs; horses
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
solution for injection
|
| International name (active substance): |
Calcium gluconate, Magnesium chloride hexahydrate, Disodium glycerophosphate
|
| 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: |
08-Apr-2014
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[DOCX] 26012021LI (26-Jan-2021)
|
| Labelling text: |
[DOCX] 26012021M (26-Jan-2021)
|
| Summary of product characteristics: |
[DOCX] 26012021ZA (26-Jan-2021)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/09/0005-01 |
|
1 |
Polipropilēna flakons, 500 ml |
-
|
|
|
Shotapen
|
-
|
V/NRP/01/1396
|
Virbac S.A., Francija
|
QJ01RA01
|
cattle; pigs; horses; dogs; cats
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/01/1396-01 |
|
1 |
Stikla flakons, 50 ml |
-
|
| V/NRP/01/1396-02 |
|
1 |
Stikla flakons, 100 ml |
-
|
| V/NRP/01/1396-03 |
|
1 |
Stikla flakons, 250 ml |
-
|
| V/NRP/01/1396-04 |
|
1 |
PET flakons, 100 ml |
-
|
| V/NRP/01/1396-05 |
|
1 |
PET flakons, 250 ml |
-
|
|
|
Arentor DC
|
250 mg
|
V/DCP/18/0054
|
Univet Ltd., Īrija
|
QJ51DB90
|
dry cows
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/DCP/18/0054-01 |
|
20 |
Injektors, 3 g/deva |
-
|
| V/DCP/18/0054-02 |
|
120 |
Injektors, 3 g/deva |
-
|
|
|
Lamoxsan
|
150 mg/ml
|
V/DCP/23/0022
|
Alfasan Nederland BV, Nīderlande
|
QJ01CA04
|
cattle; pigs
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/DCP/23/0022-01 |
|
1 |
Stikla flakons, 100 ml |
-
|
| V/DCP/23/0022-02 |
|
1 |
Stikla flakons, 250 ml |
-
|
| V/DCP/23/0022-03 |
|
1 |
PET flakons, 100 ml |
-
|
| V/DCP/23/0022-04 |
|
1 |
PET flakons, 250 ml |
-
|
|
|
Ketamine 10%
|
100 mg/ml
|
V/NRP/97/0547
|
Alfasan International B.V., Nīderlande
|
QN01AX03
|
dogs; cats
|
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 |
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] 150917LI (13-Apr-2018)
|
| Labelling text: |
[PDF] 150917M (13-Apr-2018)
|
| Summary of product characteristics: |
[PDF] 150917ZA (13-Apr-2018)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/97/0547-01 |
100 mg/ml |
1 |
Flakons, 10 ml |
-
|
| V/NRP/97/0547-02 |
100 mg/ml |
35 |
Flakons, 10 ml |
-
|
|
|
Bayvarol
|
3.6 mg
|
V/NRP/93/0024
|
Elanco Animal Health GmbH, Vācija
|
QP53AC05
|
honey bees
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/93/0024-01 |
3,6 mg |
5 |
Alumīnija folijas maisiņš, 4 plāksnītes |
-
|
| V/NRP/93/0024-02 |
3,6 mg |
200 |
Alumīnija folijas maisiņš, 4 plāksnītes |
-
|
|
|
Neurotranq
|
10 mg/ml
|
V/NRP/98/0793
|
Alfasan International B.V., Nīderlande
|
QN05AA04
|
dogs; cats
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
solution for injection
|
| International name (active substance): |
Acepromazine maleate
|
| Distribution category: |
To be used only by veterinary surgeon
|
| 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] 171117LI (19-Dec-2017)
|
| Labelling text: |
[PDF] 171117M (19-Dec-2017)
|
| Summary of product characteristics: |
[PDF] 171117ZA (19-Dec-2017)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/98/0793-01 |
10 mg/ml |
1 |
Flakons, 50 ml |
-
|
|
|
Nobilis IB+ND+EDS
|
-
|
V/NRP/96/0276
|
Intervet International B.V., Nīderlande
|
QI01AA13
|
chickens
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
emulsion for injection
|
| International name (active substance): |
Inactivated Egg Drop syndrome virus,Inactivated infectious bronchitis virus, serotype Massachusetts, strain M41,Inactivated Newcastle disease virus, strain Clone 30
|
| 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-Oct-2010
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[PDF] Skat_sadaļā_Zāļu_apraksts (06-Dec-2023)
|
| Labelling text: |
[PDF] Skat_sadaļā_Zāļu_apraksts (06-Dec-2023)
|
| Summary of product characteristics: |
[DOCX] Zāļu_informācija_ZA_M_LI (06-Dec-2023)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/96/0276-01 |
|
1 |
Stikla pudelīte, 1000 deva |
-
|
| V/NRP/96/0276-02 |
|
1 |
PET pudele, 1000 deva |
-
|
|
|
Tetrasol 20% L.A.
|
-
|
V/NRP/00/1116
|
Univet Ltd., Īrija
|
QJ01AA06
|
cattle; pigs; sheep
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
solution for injection
|
| International name (active substance): |
Oxytetracycline dihydrate
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
Univet Ltd., Īrija
|
| Date of authorisation/renewal: |
09-Mar-2010
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[PDF] 140319LI (14-Mar-2019)
|
| Labelling text: |
[PDF] 140319M (14-Mar-2019)
|
| Summary of product characteristics: |
[PDF] 140319ZA (14-Mar-2019)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/00/1116-01 |
200 mg/ml |
1 |
Stikla (tumša) flakons, 100 ml |
-
|
| V/NRP/00/1116-02 |
200 mg/ml |
12 |
Stikla (tumša) flakons, 100 ml |
-
|
|
|
Oxytocin
|
10 IU/ml
|
V/NRP/97/0549
|
Alfasan International B.V., Nīderlande
|
QH01BB02
|
cattle; pigs; sheep; goats; horses; dogs; cats
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
solution for injection
|
| International name (active substance): |
Oxytocin
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
Alfasan International B.V., Nīderlande
|
| Date of authorisation/renewal: |
18-Aug-2008
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[DOCX] 27012022LI (27-Jan-2022)
|
| Labelling text: |
[DOCX] 27012022 (27-Jan-2022)
|
| Summary of product characteristics: |
[DOCX] 27012022ZA (27-Jan-2022)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/97/0549-02 |
10 IU/ml |
1 |
Flakons, 50 ml |
-
|
|
|
BIO-MD-VAC
|
-
|
V/NRP/02/1497
|
Fatro S.p.A., Itālija
|
QI01AD03
|
chickens
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
deep frozen vaccine with solution for injection
|
| International name (active substance): |
Herpesvirus chicken
|
| 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] 88-130608LI (13-Jun-2008)
|
| Labelling text: |
[PDF] 88-130608ZA (13-Jun-2008)
|
| Summary of product characteristics: |
[PDF] 88-130608ZA (13-Jun-2008)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/02/1497-01 |
|
1 |
Stikla ampula, 1000 deva |
-
|
|
|
Stresnil
|
40 mg/ml
|
V/NRP/97/0688
|
Elanco GmbH, Vācija
|
QN05AD90
|
pigs
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/97/0688-01 |
40 mg/ml |
1 |
Flakons, 100 ml |
-
|
|
|
Surolan
|
-
|
V/NRP/96/0412
|
Elanco GmbH, Vācija
|
QD01AC52
|
dogs; cats
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
suspension for external use
|
| International name (active substance): |
Miconazole nitrate, Prednisolone acetate, Polymyxin B sulphate
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
Lusomedicamenta Sociedad Tecnica Farmaceutica, S.A. , Portugāle
|
| Date of authorisation/renewal: |
14-Aug-2012
|
| 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/96/0412-01 |
|
1 |
Polietilēna flakons, 15 ml |
-
|
| V/NRP/96/0412-02 |
|
1 |
Polietilēna flakons, 30 ml |
-
|
|
|
Apistan
|
800 mg
|
V/NRP/96/0252
|
Vita Bee Health Limited, Īrija
|
QP53AC10
|
bees
|
Vairāk
|
Medicinal product information
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/96/0252-01 |
800 mg/8 g |
10 |
Alumīnija iepakojums, 8 g/plāksnīte |
-
|
|
|
Multimast Dry Cow
|
-
|
V/NRP/00/1168
|
Bimeda Animal Health Limited, Īrija
|
QJ51RG01
|
dry cows
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
intramammary suspension
|
| International name (active substance): |
Neomycin sulphate, Procaine benzylpenicillin, Penethamate hydroiodide
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
Bimeda Animal Health Limited, Īrija
|
| Date of authorisation/renewal: |
15-Feb-2010
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[PDF] 270919LI (27-Sep-2019)
|
| Labelling text: |
[PDF] 29032019M (29-Mar-2019)
|
| Summary of product characteristics: |
[PDF] 29032019ZA (29-Mar-2019)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/00/1168-01 |
|
1 |
Injektors, 1 deva |
-
|
| V/NRP/00/1168-02 |
|
120 |
Injektors, 1 deva |
-
|
|