OXITETRACICLINA FP 900 mg/g pulbere pentru utilizare în apa de băut/înlocuitor de lapte
OXITETRACICLINA FP 900 mg/g pulbere pentru utilizare în apa de băut/înlocuitor de lapte
Authorised
- Oxytetracycline hydrochloride
Product identification
Medicine name:
OXITETRACICLINA FP 900 mg/g pulbere pentru utilizare în apa de băut/înlocuitor de lapte
Active substance:
- Oxytetracycline hydrochloride
Target species:
-
Pig
-
Cattle (suckling calf)
-
Horse (suckling foal)
-
Sheep (suckling lamb)
-
Goat (suckling kid)
-
Rabbit
-
Dog
-
Chicken (broiler)
-
Turkey
-
Duck
-
Goose
-
Chicken
-
Fish
Route of administration:
-
Buccal use
Product details
Active substance and strength:
-
Oxytetracycline hydrochloride900.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Oral powder
Withdrawal period by route of administration:
-
Buccal use
-
Pig
-
Meat and offal7day
-
-
Cattle (suckling calf)
-
Meat and offal7day
-
-
Horse (suckling foal)
-
Meat and offal7day
-
-
Sheep (suckling lamb)
-
Meat and offal7day
-
-
Goat (suckling kid)
-
Meat and offal7day
-
-
Rabbit
-
Meat and offal7day
-
-
Chicken (broiler)
-
Meat and offal7day
-
-
Turkey
-
Meat and offal7day
-
-
Duck
-
Meat and offal7day
-
-
Goose
-
Meat and offal7day
-
-
Chicken
-
Meat and offal7day
-
-
Fish
-
Meat90dayin SPC, nu sunt specificate ”Day degree”
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA06
Legal status of supply:
This information is not available for this product.
Authorisation status:
-
Valid
Authorised in:
-
Romania
Available in:
-
Romania
Package description:
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - Directive No 2001/82/EC
Marketing authorisation holder:
- Pasteur Filiala Filipesti S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Pasteur Filiala Filipesti S.A.
Responsible authority:
- Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
- 140004
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.
Romanian (PDF)
Published on: 18/06/2024