ACTI-TETRA I
ACTI-TETRA I
Authorised
- Oxytetracycline hydrochloride
Product identification
Medicine name:
ACTI-TETRA I
Active substance:
- Oxytetracycline hydrochloride
Target species:
-
Cattle
-
Pig
-
Cat
-
Horse
-
Sheep
-
Goat
-
Dog
Route of administration:
-
Intramuscular use
-
Subcutaneous use
-
Intravenous use
-
Intraperitoneal use
Product details
Active substance and strength:
-
Oxytetracycline hydrochloride53.96milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Milk3day
-
Meat and offal14day
-
-
Pig
-
Meat and offal14day
-
-
Cat
-
Horse
-
Milk3day
-
Meat and offal14day
-
-
Sheep
-
Milk3day
-
Meat and offal14day
-
-
Goat
-
Milk3day
-
Meat and offal14day
-
-
Dog
-
-
Subcutaneous use
-
Cattle
-
Milk3day
-
Meat and offal14day
-
-
Pig
-
Meat and offal14day
-
-
Cat
-
Horse
-
Milk3day
-
Meat and offal14day
-
-
Sheep
-
Milk3day
-
Meat and offal14day
-
-
Goat
-
Milk3day
-
Meat and offal14day
-
-
Dog
-
-
Intravenous use
-
Cattle
-
Milk3day
-
Meat and offal14day
-
-
Pig
-
Meat and offal14day
-
-
Cat
-
Horse
-
Milk3day
-
Meat and offal14day
-
-
Sheep
-
Milk3day
-
Meat and offal14day.
-
-
Goat
-
Milk3day
-
Meat and offal14day
-
-
Dog
-
-
Intraperitoneal use
-
Cattle
-
Milk3day
-
Meat and offal14day
-
-
Pig
-
Meat and offal14day
-
-
Cat
-
Horse
-
Milk3day
-
Meat and offal14day
-
-
Sheep
-
Milk3day
-
Meat and offal14day
-
-
Goat
-
Milk3day
-
Meat and offal14day
-
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Laboratoires Biove
Marketing authorisation date:
Manufacturing sites for batch release:
- LABORATOIRES BIOVE
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/6090637 3/1988
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.
French (PDF)
Published on: 4/04/2022
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