Taf Spray 28.5 mg/g Solution pour pulvérisation cutanée
Taf Spray 28.5 mg/g Solution pour pulvérisation cutanée
Authorised
- Thiamphenicol
Product identification
Medicine name:
Taf Spray 28.5 mg/g Solution pour pulvérisation cutanée
Taf Spray 28.5 mg/g Spray zur Anwendung auf der Haut, Lösung
Active substance:
- Thiamphenicol
Target species:
-
Cattle
-
Pig
-
Mink
-
Sheep
-
Goat
-
Horse
-
Rabbit
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Thiamphenicol28.50/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Cutaneous spray, solution
Withdrawal period by route of administration:
-
Cutaneous use
-
Cattle
-
Meat and offal0day
-
Milk0hourDo not use on the udder of lactating animals if their milk is intended for human consumption.
-
-
Pig
-
Meat and offal14day
-
-
Sheep
-
Meat and offal0day
-
Milk0hourDo not use on the udder of lactating animals if their milk is intended for human consumption.
-
-
Goat
-
Meat and offal0day
-
Milk0hourDo not use on the udder of lactating animals if their milk is intended for human consumption.
-
-
Horse
-
Meat and offal0day
-
Milk0hourDo not use on the udder of lactating animals if their milk is intended for human consumption.
-
-
Rabbit
-
Meat0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD06AX
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Luxembourg
Package description:
- Aluminium pressurised container with epoxy phenolic pigment lacquer of 400 ml
- Aluminium pressurised container with epoxy phenolic pigment lacquer of 300 ml
- Aluminium pressurised container with epoxy phenolic pigment lacquer of 200 ml
- Aluminium pressurised container with epoxy phenolic pigment lacquer of 150 ml
- Aluminium pressurised container with epoxy phenolic pigment lacquer of 50 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Dechra Regulatory B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Eurovet Animal Health B.V.
- IGS Aerosols GmbH
Responsible authority:
- Ministere De La Sante Division De La Pharmacie Et Des Medicaments
Authorisation number:
- V 914/16/01/1486
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
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in another language below.
French (PDF)
Published on: 30/06/2023
