Veterinary Medicines

GLYPHOSTAN 100 mg/ml injekčný roztok

Not authorised
  • SODIUM GLYCEROPHOSPHATE
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Product identification

Medicine name:
GLYPHOSTAN 100 mg/ml injekčný roztok
Active substance:
  • SODIUM GLYCEROPHOSPHATE
Target species:
  • Cattle
  • Sheep
  • Goat
  • Pig
  • Dog
  • Other Rodents
  • Chinchilla
  • Mink
  • Fox
  • Horse
  • Rabbit (non food-producing)
Route of administration:
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • SODIUM GLYCEROPHOSPHATE
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • All relevant tissues
        no withdrawal period
    • Sheep
      • All relevant tissues
        no withdrawal period
    • Goat
      • All relevant tissues
        no withdrawal period
    • Pig
      • All relevant tissues
        no withdrawal period
    • Dog
    • Other Rodents
    • Chinchilla
    • Mink
    • Fox
    • Horse
      • All relevant tissues
        no withdrawal period
    • Rabbit (non food-producing)
  • Subcutaneous use
    • Horse
      • All relevant tissues
        no withdrawal period
    • Cattle
      • All relevant tissues
        no withdrawal period
    • Sheep
      • All relevant tissues
        no withdrawal period
    • Goat
      • All relevant tissues
        no withdrawal period
    • Pig
      • All relevant tissues
        no withdrawal period
    • Dog
    • Other Rodents
    • Chinchilla
    • Mink
    • Fox
    • Rabbit (non food-producing)
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB05XA14
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Slovakia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • BB Pharma a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Farmácia Martin a.s.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 87/921/69-S
Date of authorisation status change:

Documents

Combined File of all Documents

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Slovak (PDF)
Published on: 18/11/2021
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