Oxy-kel 20% Long Acting 200 mg/ml Oplossing voor injectie
Oxy-kel 20% Long Acting 200 mg/ml Oplossing voor injectie
Authorised
- Oxytetracycline hydrochloride
Product identification
Medicine name:
Oxy-kel 20% Long Acting 200 mg/ml Oplossing voor injectie
Oxy-kel 20% Long Acting 200 mg/ml Solution injectable
Oxy-kel 20% Long Acting 200 mg/ml Injektionslösung
Active substance:
- Oxytetracycline hydrochloride
Target species:
-
Cattle
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Oxytetracycline hydrochloride221.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal53day
-
Milkno withdrawal periodDo not use in animals producing milk for human consumption
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Oxy-kel 20% Long Acting 1 Vial with 250 ml Solution for injection
- Oxy-kel 20% Long Acting 1 Vial with 100 ml Solution for injection
- Oxy-kel 20% Long Acting 1 Vial with 50 ml Solution for injection
- Oxy-kel 20% Long Acting 1 Vial with 30 ml Solution for injection
- Oxy-kel 20% Long Acting 25 Vials with 30 ml Solution for injection
- Oxy-kel 20% Long Acting 12 Vials with 50 ml Solution for injection
- Oxy-kel 20% Long Acting 12 Vials with 100 ml Solution for injection
- Oxy-kel 20% Long Acting 12 Vials with 250 ml Solution for injection
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:
- KELA Kempisch Laboratorium Kela Laboratoria
Marketing authorisation date:
Manufacturing sites for batch release:
- KELA Kempisch Laboratorium Kela Laboratoria
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V156213
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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Package Leaflet
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Labelling
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