Veterinary Medicines

DUPHALYTE injekčný roztok

Authorised
  • Thiamine hydrochloride
  • Riboflavin sodium phosphate dihydrate
  • Pyridoxine hydrochloride
  • Cyanocobalamin
  • Nicotinamide
  • Panthenol
  • Sodium glutamate
  • Calcium chloride hexahydrate
  • Magnesium sulfate
  • Potassium chloride
  • Glucose monohydrate
  • Leucine
  • Cysteine hydrochloride monohydrate
  • Histidine hydrochloride monohydrate
  • Isoleucine
  • Leucine
  • Methionine
  • Lysine hydrochloride
  • Phenylalanine
  • Threonine
  • Tryptophan
  • Valine
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Product identification

Medicine name:
DUPHALYTE injekčný roztok
Active substance:
  • Thiamine hydrochloride
  • Riboflavin sodium phosphate dihydrate
  • Pyridoxine hydrochloride
  • Cyanocobalamin
  • Nicotinamide
  • Panthenol
  • Sodium glutamate
  • Calcium chloride hexahydrate
  • Magnesium sulfate
  • Potassium chloride
  • Glucose monohydrate
  • Leucine
  • Cysteine hydrochloride monohydrate
  • Histidine hydrochloride monohydrate
  • Isoleucine
  • Leucine
  • Methionine
  • Lysine hydrochloride
  • Phenylalanine
  • Threonine
  • Tryptophan
  • Valine
Target species:
  • Horse
  • Cattle
  • Dog
  • Cat
  • Pig
  • Chicken (one day-old chick)
Route of administration:
  • Intravenous use
  • Subcutaneous use
  • Intraperitoneal use

Product details

Active substance and strength:
  • Thiamine hydrochloride
    0.10
    milligram(s)
    /
    1.00
    millilitre(s)
  • Riboflavin sodium phosphate dihydrate
    0.04
    milligram(s)
    /
    1.00
    millilitre(s)
  • Pyridoxine hydrochloride
    0.10
    milligram(s)
    /
    1.00
    millilitre(s)
  • Cyanocobalamin
    0.05
    microgram(s)
    /
    1.00
    millilitre(s)
  • Nicotinamide
    1.50
    milligram(s)
    /
    1.00
    millilitre(s)
  • Panthenol
    0.05
    milligram(s)
    /
    1.00
    millilitre(s)
  • Sodium glutamate
    0.04
    milligram(s)
    /
    1.00
    millilitre(s)
  • Calcium chloride hexahydrate
    0.23
    milligram(s)
    /
    1.00
    millilitre(s)
  • Magnesium sulfate
    0.29
    milligram(s)
    /
    1.00
    millilitre(s)
  • Potassium chloride
    0.20
    milligram(s)
    /
    1.00
    milligram(s)
  • Glucose monohydrate
    45.56
    milligram(s)
    /
    1.00
    millilitre(s)
  • Leucine
    0.03
    milligram(s)
    /
    1.00
    millilitre(s)
  • Cysteine hydrochloride monohydrate
    0.01
    milligram(s)
    /
    1.00
    millilitre(s)
  • Histidine hydrochloride monohydrate
    0.01
    milligram(s)
    /
    1.00
    millilitre(s)
  • Isoleucine
    0.01
    milligram(s)
    /
    1.00
    millilitre(s)
  • Leucine
    0.04
    milligram(s)
    /
    1.00
    millilitre(s)
  • Methionine
    0.01
    milligram(s)
    /
    1.00
    millilitre(s)
  • Lysine hydrochloride
    0.03
    milligram(s)
    /
    1.00
    millilitre(s)
  • Phenylalanine
    0.03
    milligram(s)
    /
    1.00
    millilitre(s)
  • Threonine
    0.02
    milligram(s)
    /
    1.00
    millilitre(s)
  • Tryptophan
    0.01
    milligram(s)
    /
    1.00
    millilitre(s)
  • Valine
    0.05
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Horse
      • Meat and offal
        0
        day
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig
      • Meat and offal
        0
        day
  • Intraperitoneal use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB05BA10
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovakia
Available 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:
  • Zoetis Ceska Republika s.r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Manufacturing & Research Spain, S.L.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/760/94-S
Date of authorisation status change:

Documents

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Published on: 13/12/2021
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