SPECTAM SOLUTION INJECTABLE
SPECTAM SOLUTION INJECTABLE
Authorised
- Spectinomycin dihydrochloride pentahydrate
Product identification
Medicine name:
SPECTAM SOLUTION INJECTABLE
Active substance:
- Spectinomycin dihydrochloride pentahydrate
Target species:
-
Cattle
-
Pig
-
Horse
-
Horse (mare)
-
Sheep
-
Goat
-
Poultry
Route of administration:
-
Intramuscular use
-
Subcutaneous use
-
Endosinusial use
Product details
Active substance and strength:
-
Spectinomycin dihydrochloride pentahydrate116.40/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal30day
-
Milk3day
-
-
Pig
-
Meat and offal30day
-
-
Horse
-
Meat and offal30day
-
-
Horse (mare)
-
Milk3day
-
-
Sheep
-
Meat and offal30day
-
Milk3day
-
-
Goat
-
Meat and offal30day
-
Milk3day
-
-
Poultry
-
Eggsno withdrawal periodEn l'absence de LMR pour les œufs, ne pas utiliser chez les espèces pondeuses productrices d'œufs de consommation, 4 semaines avant le démarrage de la ponte et pendant celle-ci.
-
Meat and offal30day
-
-
-
Subcutaneous use
-
Poultry
-
Meat and offal30day
-
Eggsno withdrawal periodEn l'absence de LMR pour les œufs, ne pas utiliser chez les espèces pondeuses productrices d'œufs de consommation, 4 semaines avant le démarrage de la ponte et pendant celle-ci.
-
-
-
Endosinusial use
-
Poultry
-
Meat and offal30day
-
Eggsno withdrawal periodEn l'absence de LMR pour les œufs, ne pas utiliser chez les espèces pondeuses productrices d'œufs de consommation, 4 semaines avant le démarrage de la ponte et pendant celle-ci.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01XX04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva Sante Animale
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/1512729 5/1992
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
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in another language below.
French (PDF)
Published on: 4/04/2022