Veterinary Medicines

Duphalyte oldatos injekció A.U.V.

Authorised
  • Potassium chloride
  • Thiamine
  • Riboflavin
  • VITAMIN B6
  • VITAMIN B12
  • Dexpanthenol
  • PHENYLALANINE DL
  • DL-Tryptophan
  • DL-Valine
  • Calcium chloride hexahydrate
  • Magnesium sulfate
  • GLUCOSE, ANHYDROUS
  • L-arginine hydrochloride
  • L-CYSTEINE HYDROCHLORIDE MONOHYDRATE
  • L-histidine hydrochloride
  • L-ISOLEUCINE
  • L-LEUCINE
  • L-lysine hydrochloride
  • L-METHIONINE
  • L-THREONINE
  • Nicotinamide
  • SODIUM L-GLUTAMATE
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Product identification

Medicine name:
Duphalyte oldatos injekció A.U.V.
Active substance:
  • Potassium chloride
  • Thiamine
  • Riboflavin
  • VITAMIN B6
  • VITAMIN B12
  • Dexpanthenol
  • PHENYLALANINE DL
  • DL-Tryptophan
  • DL-Valine
  • Calcium chloride hexahydrate
  • Magnesium sulfate
  • GLUCOSE, ANHYDROUS
  • L-arginine hydrochloride
  • L-CYSTEINE HYDROCHLORIDE MONOHYDRATE
  • L-histidine hydrochloride
  • L-ISOLEUCINE
  • L-LEUCINE
  • L-lysine hydrochloride
  • L-METHIONINE
  • L-THREONINE
  • Nicotinamide
  • SODIUM L-GLUTAMATE
Target species:
  • Cattle
  • Pig
  • Horse
  • Dog
  • Cat
  • Chicken (hen)
Route of administration:
  • Intraperitoneal use
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Potassium chloride
    0.20
    milligram(s)
    /
    1.00
    millilitre(s)
  • Thiamine
    0.20
    milligram(s)
    /
    1.00
    millilitre(s)
  • Riboflavin
    0.08
    milligram(s)
    /
    1.00
    millilitre(s)
  • VITAMIN B6
    0.20
    milligram(s)
    /
    1.00
    millilitre(s)
  • VITAMIN B12
    0.10
    microgram(s)
    /
    1.00
    millilitre(s)
  • Dexpanthenol
    0.10
    milligram(s)
    /
    1.00
    millilitre(s)
  • PHENYLALANINE DL
    0.03
    milligram(s)
    /
    1.00
    millilitre(s)
  • DL-Tryptophan
    0.01
    milligram(s)
    /
    1.00
    millilitre(s)
  • DL-Valine
    0.05
    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)
  • GLUCOSE, ANHYDROUS
    45.56
    milligram(s)
    /
    1.00
    millilitre(s)
  • L-arginine hydrochloride
    0.03
    milligram(s)
    /
    1.00
    millilitre(s)
  • L-CYSTEINE HYDROCHLORIDE MONOHYDRATE
    0.01
    milligram(s)
    /
    1.00
    millilitre(s)
  • L-histidine hydrochloride
    0.01
    milligram(s)
    /
    1.00
    millilitre(s)
  • L-ISOLEUCINE
    0.01
    milligram(s)
    /
    1.00
    millilitre(s)
  • L-LEUCINE
    0.04
    milligram(s)
    /
    1.00
    millilitre(s)
  • L-lysine hydrochloride
    0.03
    milligram(s)
    /
    1.00
    millilitre(s)
  • L-METHIONINE
    0.01
    milligram(s)
    /
    1.00
    millilitre(s)
  • L-THREONINE
    0.02
    milligram(s)
    /
    1.00
    millilitre(s)
  • Nicotinamide
    2.25
    milligram(s)
    /
    1.00
    millilitre(s)
  • SODIUM L-GLUTAMATE
    0.04
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intraperitoneal use
    • Cattle
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
  • Intravenous use
    • Cattle
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Chicken (hen)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA11EX
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Hungary
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Zoetis Hungary Kft.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Manufacturing & Research Spain, S.L.
Responsible authority:
  • Directorate Of Veterinary Medicinal Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Hungarian (PDF)
Published on: 3/04/2024
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Package Leaflet

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Hungarian (PDF)
Published on: 3/04/2024
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Labelling

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Hungarian (PDF)
Published on: 3/04/2024
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