Veterinary Medicines

Vitamin-E-Selen ad us.vet.

Authorised
  • DL-ALPHA TOCOPHEROL ACETATE
  • Sodium selenite
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Product identification

Medicine name:
Vitamin-E-Selen ad us.vet.
Active substance:
  • DL-ALPHA TOCOPHEROL ACETATE
  • Sodium selenite
Target species:
  • Cattle
  • Goat
  • Sheep
  • Horse
  • Pig
Route of administration:
  • Subcutaneous use
  • Intramuscular use

Product details

Active substance and strength:
  • DL-ALPHA TOCOPHEROL ACETATE
    150.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Sodium selenite
    1.10
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Meat and offal
        7
        day
      • Milk
        0
        day
    • Goat
      • Milk
        0
        day
      • Meat and offal
        7
        day
    • Sheep
      • Milk
        0
        day
      • Meat and offal
        7
        day
    • Horse
      • Milk
        0
        day
      • Meat and offal
        7
        day
    • Pig
      • Meat and offal
        7
        day
  • Intramuscular use
    • Cattle
      • Meat and offal
        7
        day
      • Milk
        0
        day
    • Goat
      • Milk
        0
        day
      • Meat and offal
        7
        day
    • Sheep
      • Meat and offal
        7
        day
      • Milk
        0
        day
    • Horse
      • Milk
        0
        day
      • Meat and offal
        7
        day
    • Pig
      • Meat and offal
        7
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA11JB
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Available in:
  • Germany
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
  • aniMedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • aniMedica GmbH
Responsible authority:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • 6673147.00.00
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
German (RTF)
Published on: 3/06/2024
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 3/06/2024
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Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 14/10/2024
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