L.S. Injection solution for injection for calves (pre-ruminant), sheep, goats, pigs, birds and dogs
L.S. Injection solution for injection for calves (pre-ruminant), sheep, goats, pigs, birds and dogs
Authorised
- Lincomycin hydrochloride monohydrate
- Spectinomycin dihydrochloride pentahydrate
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 monohydrate50.00milligram(s)1.00millilitre(s)
-
Spectinomycin dihydrochloride pentahydrate100.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle (pre-ruminant)
-
Meat14day
-
Liver21day
-
Kidney21day
-
-
Sheep
-
Meat14dayНе се разрешава за употреба при животни, чието мляко е предназначено за човешка консумация.
-
Liver21day
-
Kidney21day
-
-
Goat
-
Meat14dayНе се разрешава за употреба при животни, чието мляко е предназначено за човешка консумация.
-
Liver21day
-
Kidney21day
-
-
Pig
-
Meat14day
-
Liver21day
-
Kidney14day
-
-
Dog
-
-
Subcutaneous use
-
Chicken
-
Meat14dayНе се разрешава употребата при птици, чиито яйца са предназначени за човешка консумация
-
Liver21day
-
Kidney21day
-
-
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
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:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 17/12/2024
Labelling
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in another language below.
Bulgarian (PDF)
Published on: 17/12/2024
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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