PAN TERRAMICINA
PAN TERRAMICINA
Authorised
- Oxytetracycline
Product identification
Medicine name:
PAN TERRAMICINA
Active substance:
- Oxytetracycline
Target species:
-
Dog
-
Horse
-
Cat
-
Turkey
-
Chicken (broiler)
-
Chicken
-
Cattle
Route of administration:
-
Ocular use
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
-
Cutaneous use
-
Intrauterine use
Product details
Active substance and strength:
-
Oxytetracycline30.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Ocular use
-
Dog
-
Horse
-
Meat and offal20dayUso non autorizzato in equidi che producono latte per il consumo umano
-
-
Cat
-
-
Intramuscular use
-
Horse
-
Meat and offal20dayUso non autorizzato in equidi che producono latte per il consumo umano
-
-
-
Intravenous use
-
Horse
-
Meat and offal20dayUso non autorizzato in equidi che producono latte per il consumo umano
-
-
-
Subcutaneous use
-
Turkey
-
Meat and offal15dayUso non autorizzato in uccelli che producono uova per il consumo umano
-
-
Chicken (broiler)
-
Meat and offal15dayUso non autorizzato in uccelli che producono uova per il consumo umano
-
-
Chicken
-
Meat and offal15dayUso non autorizzato in uccelli che producono uova per il consumo umano
-
-
Horse
-
Meat and offal20dayUso non autorizzato in equidi che producono latte per il consumo umano
-
-
-
Cutaneous use
-
Dog
-
Horse
-
Meat and offal20dayUso non autorizzato in equidi che producono latte per il consumo umano
-
-
Cat
-
-
Intrauterine use
-
Cattle
-
Milk12hour
-
Meat and offal4day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Available in:
-
Italy
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:
- Zoetis Italia S.r.l
Marketing authorisation date:
Manufacturing sites for batch release:
- Fareva Amboise
Responsible authority:
- Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
This document does not exist in this language (English). You can find it
in another language below.
Italian (PDF)
Published on: 3/06/2022
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