TETRAVET L.A, 200mg/ml, Injekční roztok
TETRAVET L.A, 200mg/ml, Injekční roztok
Authorised
- Oxytetracycline dihydrate
Product identification
Medicine name:
TETRAVET L.A, 200mg/ml, Injekční roztok
Active substance:
- Oxytetracycline dihydrate
Target species:
-
Sheep
-
Pig
-
Cattle
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Oxytetracycline dihydrate215.60milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Sheep
-
Meat and offal28day
-
Milkno withdrawal periodNepoužívat u ovcí, jejichž mléko je určeno pro lidskou spotřebu.,
-
-
Pig
-
Meat and offal16day
-
-
Cattle
-
Meat and offal26day
-
Milk7day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Czechia
Available in:
-
Czechia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Ceva Animal Health Slovakia s.r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- CEVA Santé Animale
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/027/94-C
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
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 24/04/2023
Package Leaflet
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in another language below.
Czech (PDF)
Published on: 24/04/2023
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 24/04/2023
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