ENGEMYCIN 10% LA, ενέσιμο διάλυμα για βοοειδή, πρόβατα, χοίρους, σκύλους και γάτες
ENGEMYCIN 10% LA, ενέσιμο διάλυμα για βοοειδή, πρόβατα, χοίρους, σκύλους και γάτες
Authorised
- Oxytetracycline
Product identification
Medicine name:
ENGEMYCIN 10% LA, ενέσιμο διάλυμα για βοοειδή, πρόβατα, χοίρους, σκύλους και γάτες
Active substance:
- Oxytetracycline
Target species:
-
Cattle
-
Sheep
-
Pig
-
Dog
-
Cat
Route of administration:
-
Intramuscular and intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Oxytetracycline100.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular and intravenous use
-
Cattle
-
Meat and offal27dayχαμηλή δοσολογία
-
Milk96hour8 αμέλξεις/ χαμηλή δοσολογία
-
Meat and offal18dayυψηλή δοσολογία
-
-
Sheep
-
Meat and offal24dayχαμηλή δοσολογία
-
Milk96hour8 αμέλξεις/ χαμηλή δοσολογία
-
Meat and offal18dayυψηλή δοσολογία
-
-
Pig
-
Meat and offal8dayχαμηλή δοσολογία
-
Meat and offal7dayυψηλή δοσολογία
-
-
Dog
-
Cat
-
-
Subcutaneous use
-
Cattle
-
Meat and offal27dayχαμηλή δοσοσλογία
-
Milk96hourχαμηλή δοσοσλογία
-
Meat and offal18dayυψηλή δοσολογία
-
-
Sheep
-
Meat and offal24dayχαμηλή δοσοσλογία
-
Milk96hourχαμηλή δοσοσλογία
-
Meat and offal18dayυψηλή δοσολογία
-
-
Pig
-
Meat and offal8dayχαμηλή δοσοσλογία
-
Meat and offal7dayυψηλή δοσολογία
-
-
Dog
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone)
Marketing authorisation holder:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International GmbH
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 65435/14-09-2012/11-02-2013/K-0058202)
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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