Oxytetracycline 200 mg/ml L.A. solution for injection for cattle
Oxytetracycline 200 mg/ml L.A. solution for injection for cattle
Authorised
- Oxytetracycline hydrochloride
Product identification
Medicine name:
Oxytetracycline 200 mg/ml L.A. solution for injection for cattle
Active substance:
- Oxytetracycline hydrochloride
Target species:
-
Cattle
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Oxytetracycline hydrochloride215.86/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal28day
-
Milk10day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Available in:
-
Ireland
Package description:
- Brown glass vial 100 ml, type II, with a bromobutyl rubber closure, sealed with an aluminium cap containing 100 ml ofproduct.The vials are packed in a polystyrene box, 12 vials of 100 ml per box, with 12 package leaflets.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Informed consent (abridged application) - Council Directive 81/851/EEC
Marketing authorisation holder:
- KELA Kempisch Laboratorium Kela Laboratoria
Marketing authorisation date:
Manufacturing sites for batch release:
- KELA Kempisch Laboratorium Kela Laboratoria
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10981/005/001
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
English (PDF)
Download Published on: 25/09/2024