ENROXIL 50 mg/ml, injekcinis tirpalas
ENROXIL 50 mg/ml, injekcinis tirpalas
Authorised
- Enrofloxacin
Product identification
Medicine name:
ENROXIL 50 mg/ml, injekcinis tirpalas
Active substance:
- Enrofloxacin
Target species:
-
Cattle (calf)
-
Pig
-
Sheep
-
Goat
-
Dog
Route of administration:
-
Intravenous use
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Enrofloxacin50.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Cattle (calf)
-
Meat and offal5dayNot authorized for use in females producing milk for human consumption.
-
-
-
Intramuscular use
-
Pig
-
Meat and offal13day
-
-
-
Subcutaneous use
-
Cattle (calf)
-
Meat and offal12dayNot authorized for use in females producing milk for human consumption.
-
-
Sheep
-
Meat and offal4day
-
Milk3day
-
-
Goat
-
Meat and offal6day
-
Milk4day
-
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Package description:
- Available only in Lithuanian
- Available only in Lithuanian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- KRKA tovarna zdravil d.d. Novo mesto
Marketing authorisation date:
Manufacturing sites for batch release:
- KRKA tovarna zdravil d.d. Novo mesto
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/94/0125/001-002
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
RV0125.pdf
Lithuanian (PDF)
Download Published on: 21/06/2022
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