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Veterinary Medicines

Vitamine B-complex pro inj., oplossing voor injectie

Pooblaščeno
  • Cyanocobalamin
  • RIBOFLAVIN SODIUM PHOSPHATE
  • Pyridoxine hydrochloride
  • Nicotinamide
  • Thiamine hydrochloride
  • Ascorbic acid

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
Withdrawal period by route of administration:
  • intramuskularna uporaba
    • govedo
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • tele
      • Meat and offal
        no withdrawal period
    • Horse
      • Meat and offal
        no withdrawal period
    • Pig (sow)
      • Meat and offal
        no withdrawal period
    • Pig (piglet)
      • Meat and offal
        no withdrawal period
    • Horse (foal)
      • Meat and offal
        no withdrawal period
    • Dog
    • Cat
  • Subkutana uporaba
    • govedo
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • tele
      • Meat and offal
        no withdrawal period
    • Horse
      • Meat and offal
        no withdrawal period
    • Pig (sow)
      • Meat and offal
        no withdrawal period
    • Pig (piglet)
      • Meat and offal
        no withdrawal period
    • Horse (foal)
      • Meat and offal
        no withdrawal period
    • Dog
    • Cat
Anatomsko-terapevtsko-kemična veterinarska oznaka (ATCvet):
  • QA11EB
Status dovoljenja:
  • Valid
Opis ovojnine:

Dodatne informacije

Imetnik dovoljenja za promet z zdravilom:
  • Alfasan Nederland B.V.
Marketing authorisation date:
Proizvodna mesta, odgovorna za sproščanje serij:
  • Alfasan Nederland B.V.
Pristojni organ:
  • Medicines Evaluation Board
Številka dovoljenja :
  • REG NL 1968
Datum spremembe statusa dovoljenja:

Dokumenti

Combined File of all Documents

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Dutch (PDF)
Objavljeno na: 16/02/2022
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