Veterinary Medicines

L.S. Injection solution for injection for calves (pre-ruminant), sheep, goats, pigs, birds and dogs

Authorised
  • Lincomycin hydrochloride monohydrate
  • Spectinomycin dihydrochloride pentahydrate
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Product identification

Medicine name:
L.S. Injection инжекционен разтвор за телета (с неразвити предстомашия), овце, кози, прасета, птици и кучета
L.S. Injection solution for injection for calves (pre-ruminant), sheep, goats, pigs, birds and dogs
Active substance:
  • Lincomycin hydrochloride monohydrate
  • Spectinomycin dihydrochloride pentahydrate
Target species:
  • Cattle (pre-ruminant)
  • Sheep
  • Goat
  • Pig
  • Dog
  • Chicken
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Lincomycin hydrochloride monohydrate
    50.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Spectinomycin dihydrochloride pentahydrate
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle (pre-ruminant)
      • Meat
        14
        day
      • Liver
        21
        day
      • Kidney
        21
        day
    • Sheep
      • Meat
        14
        day
      • Liver
        21
        day
      • Kidney
        21
        day
    • Goat
      • Meat
        14
        day
      • Liver
        21
        day
      • Kidney
        21
        day
    • Pig
      • Meat
        14
        day
      • Liver
        21
        day
      • Kidney
        14
        day
  • Subcutaneous use
    • Chicken
      • Meat
        14
        day
      • Liver
        21
        day
      • Kidney
        21
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01FF52
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Bulgaria
Available in:
  • Bulgaria
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Bibliographical application (stand-alone)
Marketing authorisation holder:
  • Kepro B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Kepro B.V.
Responsible authority:
  • Bulgarian Food Safety Authority
Authorisation number:
  • 0022-2528
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Bulgarian (PDF)
Published on: 17/12/2024
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Labelling

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Bulgarian (PDF)
Published on: 17/12/2024
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 17/12/2024
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