CLORIVEN 20 mg/ml SUSPENSION PARA PULVERIZACION CUTANEA
CLORIVEN 20 mg/ml SUSPENSION PARA PULVERIZACION CUTANEA
Authorised
- Chlortetracycline hydrochloride
Product identification
Medicine name:
CLORIVEN 20 mg/ml SUSPENSION PARA PULVERIZACION CUTANEA
Active substance:
- Chlortetracycline hydrochloride
Target species:
-
Cattle
-
Sheep
-
Goat
-
Horse
-
Pig
-
Dog
-
Cat
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Chlortetracycline hydrochloride21.50/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Cutaneous spray, suspension
Withdrawal period by route of administration:
-
Cutaneous use
-
Cattle
-
Meat and offal0day
-
Milkno withdrawal periodLeche:cero días.No usar en ubres de animales lactantes si la leche se destina al consumo humano
-
-
Sheep
-
Meat and offal0day
-
Milkno withdrawal periodLeche:cero días.No usar en ubres de animales lactantes si la leche se destina al consumo humano
-
-
Goat
-
Meat and offal0day
-
Milkno withdrawal periodLeche:cero días.No usar en ubres de animales lactantes si la leche se destina al consumo humano
-
-
Horse
-
Meat and offal0day
-
Milkno withdrawal periodLeche:cero días.No usar en ubres de animales lactantes si la leche se destina al consumo humano
-
-
Pig
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD06AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Spain
Package description:
- Available only in Spanish
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Informed consent application (Article 13c of Directive No 2001/82/EC)
Marketing authorisation holder:
- Laboratorios E Industrias Iven S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios E Industrias Iven S.A.
Responsible authority:
- Spanish Agency For Medicines And Health Products
Authorisation number:
- 2982 ESP
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.
Spanish (PDF)
Published on: 9/11/2022
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 29/11/2023
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Spanish (PDF)
Published on: 9/11/2022