E-SELENSOL 70/1 mg/ml emulsion for injection for cattle, sheep and pigs
  • Tokoferol-alfa (E 307)
  • Nātrija selenīts
  • Valid
Authorised in these countries:
  • Cyprus
  • Estonia
  • Croatia
  • Greece
  • Latvia
  • Lithuania
  • Hungary
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Product identification

Medicine name:
E-SELENSOL 70/1 mg/ml emulsion for injection for cattle, sheep and pigs
E-SELENSOL 70/1 mg/ml, injekcinė emulsija galvijams, avims ir kiaulėms
Active substance and strength:
  • Tokoferol-alfa (E 307)
  • Nātrija selenīts
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA12CE99
Authorisation number:
  • LT/2/21/2656/001-002
Product identification number:
  • 84e39cc3-def1-489a-89de-9984ef4ce1e3
Permanent identification number:
  • 600000038605

Product details

Legal status of supply:
This information is not available for this product.
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        14
        day
    • Pig
      • Meat and offal
        14
        day
    • Sheep
      • Meat and offal
        30
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        14
        day
    • Pig
      • Meat and offal
        14
        day
    • Sheep
      • Meat and offal
        30
        day

Availability

Package description:
  • Type II amber coloured glass vials, with bromobutyl rubber stopper and lacquered aluminium cap. Carton box with 1 vial of 50 ml.
  • Type II amber coloured glass vials, with bromobutyl rubber stopper and lacquered aluminium cap. Carton box with 1 vial of 100 ml
Manufacturing sites for batch release:
  • Labiana Life Sciences S.A.
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.

Authorisation details

Authorisation status:
  • Valid
Authorisation procedure type:
  • Marketing Authorisation
Procedure number:
  • HU/V/0143/001/DC
Date of authorisation status change:
Legal basis of product authorisation:
  • Generic (abridged application) - art 13(1)
Authorisation country:
  • Lithuania
Responsible authority:
  • SFVS
Marketing authorisation holder:
  • Labiana
Marketing authorisation issued:
Reference member state:
  • Hungary
Concerned member states:
  • Croatia
  • Cyprus
  • Estonia
  • Greece
  • Latvia
  • Lithuania
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.

Additional information

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Documents

Other Product Information (PDF)
First published:
Last updated:
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