Veterinary Medicines

Myogaster-E Oplossing voor injectie

Authorised
  • DL-ALPHA TOCOPHEROL ACETATE
  • SODIUM SELENITE ANHYDROUS
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Product identification

Medicine name:
Myogaster-E Oplossing voor injectie
Myogaster-E Solution injectable
Myogaster-E Injektionslösung
Active substance:
  • DL-ALPHA TOCOPHEROL ACETATE
  • SODIUM SELENITE ANHYDROUS
Target species:
  • Sheep
  • Cattle (calf)
  • Pig
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • DL-ALPHA TOCOPHEROL ACETATE
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • SODIUM SELENITE ANHYDROUS
    1.32
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Sheep
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
      • Milk
        no withdrawal period
    • Cattle (calf)
      • Meat and offal
        no withdrawal period
    • Pig
      • Meat and offal
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA11JB
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Available in:
  • Belgium
Package description:
  • Myogaster-E 100 ml Vial Solution for injection
  • Myogaster-E 50 ml Vial Solution for injection
  • Myogaster-E 20 ml Vial Solution for injection

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • V.M.D.
Marketing authorisation date:
Manufacturing sites for batch release:
  • V.M.D.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V137855
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Dutch (PDF)
Published on: 28/01/2025
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French (PDF)
Published on: 28/01/2025
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Package Leaflet

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Dutch (PDF)
Published on: 28/01/2025
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French (PDF)
Published on: 28/01/2025
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German (PDF)
Published on: 28/01/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 28/01/2025
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French (PDF)
Published on: 28/01/2025
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German (PDF)
Published on: 28/01/2025
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