Vitamine B-complex pro inj., oplossing voor injectie

Ima dovoljenje za promet

Cyanocobalamin
RIBOFLAVIN SODIUM PHOSPHATE
Pyridoxine hydrochloride
Nicotinamide
Thiamine hydrochloride
Ascorbic acid

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Informacije o zdravilu

Ime zdravila:

Vitamine B-complex pro inj., oplossing voor injectie

Učinkovina:

Na voljo samo v English
Na voljo samo v English
Na voljo samo v English
Na voljo samo v English
Na voljo samo v English
Na voljo samo v English

Ciljne živalske vrste:

govedo
tele
Na voljo samo v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian
Na voljo samo v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian
Na voljo samo v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian
Na voljo samo v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Norwegian
Na voljo samo v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian
Na voljo samo v Bulgarian Spanish Czech Danish German Estonian Greek English French Italian Latvian Lithuanian Hungarian Dutch Romanian Finnish Swedish Icelandic Norwegian

Pot uporabe:

intramuskularna uporaba
Subkutana uporaba

Podatki o zdravilu

Učinkovina / Jakost:

Na voljo samo v English

2.00

microgram(s)

/

1.00

millilitre(s)
Na voljo samo v English

0.69

milligram(s)

/

1.00

millilitre(s)
Na voljo samo v English

7.00

milligram(s)

/

1.00

millilitre(s)
Na voljo samo v English

23.00

milligram(s)

/

1.00

millilitre(s)
Na voljo samo v English

35.00

milligram(s)

/

1.00

millilitre(s)
Na voljo samo v English

70.00

milligram(s)

/

1.00

millilitre(s)

Farmacevtska oblika:

Raztopina za injiciranje

Karenca glede na pot uporabe:

intramuskularna uporaba
- govedo
  - Milk
    
    no withdrawal period
    
    should be 0 days
  - Meat and offal
    
    no withdrawal period
    
    should be 0 days
- tele
  - Meat and offal
    
    no withdrawal period
    
    should be 0 days
- Horse
  - Meat and offal
    
    no withdrawal period
    
    should be 0 days
- Pig (sow)
  - Meat and offal
    
    no withdrawal period
    
    should be 0 days
- Pig (piglet)
  - Meat and offal
    
    no withdrawal period
    
    should be 0 days
- Horse (foal)
  - Meat and offal
    
    no withdrawal period
    
    should be 0 days
Subkutana uporaba
- govedo
  - Milk
    
    no withdrawal period
    
    should be 0 days
  - Meat and offal
    
    no withdrawal period
    
    should be 0 days
- tele
  - Meat and offal
    
    no withdrawal period
    
    should be 0 days
- Horse
  - Meat and offal
    
    no withdrawal period
    
    should be 0 days
- Pig (sow)
  - Meat and offal
    
    no withdrawal period
    
    should be 0 days
- Pig (piglet)
  - Meat and offal
    
    no withdrawal period
    
    should be 0 days
- Horse (foal)
  - Meat and offal
    
    no withdrawal period
    
    should be 0 days

Anatomsko-terapevtsko-kemična veterinarska oznaka klasifikacija zdravil, ki se uporabljajo v veterini (ATCvet):

QA11EB

Pravni status za dobavo/izdajo zdravila:

Zdravilo, ki se izdaja na veterinarski recept

Status dovoljenja za promet z zdravilom:

Valid

Ima dovoljenje za promet v:

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Opis ovojnine zdravila:

Na voljo samo v Dutch

Dodatne informacije

Vrsta dovoljenja:

Na voljo samo v English French Croatian Italian Latvian Finnish Swedish Icelandic Norwegian

Pravna podlaga za izdajo dovoljenja za promet z zdravilom:

Na voljo samo v English French Italian Latvian Norwegian

Imetnik dovoljenja za promet z zdravilom:

Alfasan Nederland B.V.

Datum dovoljenja za promet z zdravilom:

8/09/1992

Proizvodna mesta, odgovorna za sproščanje serij:

Alfasan Nederland B.V.

Pristojni organ:

Medicines Evaluation Board

Številka dovoljenja za promet z zdravilom:

REG NL 1968

Datum spremembe statusa dovoljenja za promet:

7/09/2016

Za poročila o domnevnih neželenih učinkih zdravil za uporabo v veterinaski medicini obiščite stran: www.adrreports.eu/vet

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