Veterinary Medicines

Myogaster-E (100 mg + 1,315 mg)/ml Roztwór do wstrzykiwań

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

Medicine name:
Myogaster-E (100 mg + 1,315 mg)/ml Roztwór do wstrzykiwań
Active substance:
  • DL-ALPHA TOCOPHEROL ACETATE
  • SODIUM SELENITE ANHYDROUS
Target species:
  • Sheep
  • Pig
  • Cattle
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • DL-ALPHA TOCOPHEROL ACETATE
    100.00
    milligram(s)/millilitre
    /
    1.00
    milligram(s)/millilitre
  • 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
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Cattle
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA11JB
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
Available in:
  • Poland
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
  • V.M.D.
Marketing authorisation date:
Manufacturing sites for batch release:
  • VMD N.V.
Responsible authority:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 1961
Date of authorisation status change:

Documents

Package Leaflet

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Polish (PDF)
Published on: 11/02/2025
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Labelling

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Polish (PDF)
Published on: 11/02/2025
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 11/02/2025
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