BACOLAM 100 mg/ml + 250.000 UI/ml sospensione iniettabile per bovini, ovi-caprini, suini, equini e tacchini
BACOLAM 100 mg/ml + 250.000 UI/ml sospensione iniettabile per bovini, ovi-caprini, suini, equini e tacchini
Authorised
- Amoxicillin
- COLISTIN SULFATE
Product identification
Medicine name:
BACOLAM 100 mg/ml + 250.000 UI/ml sospensione iniettabile per bovini, ovi-caprini, suini, equini e tacchini
Active substance:
- Amoxicillin
- COLISTIN SULFATE
Target species:
-
Cattle
-
Goat
-
Sheep
-
Pig
-
Horse (non food-producing)
-
Turkey
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Amoxicillin100.00/milligram(s)1.00millilitre(s)
-
COLISTIN SULFATE250000.00/international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal28dayNon somministrare in animali in lattazione il cui latte o derivati siano destinati al consumo umano
-
-
Goat
-
Meat and offal28dayNon somministrare in animali in lattazione il cui latte o derivati siano destinati al consumo umano
-
-
Sheep
-
Meat and offal28dayNon somministrare in animali in lattazione il cui latte o derivati siano destinati al consumo umano
-
-
Pig
-
Meat and offal13day
-
-
-
Subcutaneous use
-
Turkey
-
Meat and offal25dayUso non consentito in animali che producono uova destinati al consumo umano
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01RA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Italian (PDF)
Published on: 18/09/2024
