Ridacox 50 mg/ml oral suspension for cattle and sheep
Ridacox 50 mg/ml oral suspension for cattle and sheep
Authorised
- Toltrazuril
Product identification
Medicine name:
Ridacox 50 mg/ml oral suspension for cattle and sheep
Active substance:
- Toltrazuril
Target species:
-
Cattle
-
Sheep
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Toltrazuril50.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
Oral use
-
Cattle
-
Meat and offal63day
-
Milkno withdrawal periodNot authorised for use in animals producing milk for human consumption.
-
-
Sheep
-
Meat and offal42day
-
Milkno withdrawal periodNot authorised for use in animals producing milk for human consumption.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP51BC01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- Bottle (HDPE), closure (HDPE), sealing liner (LDPE): 250 ml of oral suspension in a box.
- Bottle (HDPE), closure (HDPE), sealing liner (LDPE): 1000 ml of oral suspension in a box.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 10(1) of Directive No 2001/83/EC)
Marketing authorisation holder:
- J & M Veterinary Services Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- KRKA tovarna zdravil d.d. Novo mesto
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10954/012/001
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
