Redymox 150 mg/ml suspension for injection for cattle, sheep, pigs, dogs and cats
Redymox 150 mg/ml suspension for injection for cattle, sheep, pigs, dogs and cats
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Redymox 150 mg/ml suspension for injection for cattle, sheep, pigs, dogs and cats
Redymox 150 mg/ml suspension for injection for cattle, sheep, pigs, dogs and cats
Active substance:
- Amoxicillin trihydrate
Target species:
-
Cattle
-
Dog
-
Sheep
-
Cat
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Amoxicillin trihydrate172.10/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal18day
-
Milk48hour
-
-
Sheep
-
Meat and offal7day
-
-
Pig
-
Meat and offal14day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal18day
-
Milk48hour
-
-
Sheep
-
Meat and offal7day
-
-
Pig
-
Meat and offal14day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- 100 ml clear, colourless Type II glass vial, closed with nitrile rubber bung and aluminium overseal. 100 ml vial in a cardboard box.
- 100 ml clear, colourless Type II glass vial, closed with nitrile rubber bung and aluminium overseal. 12 x 100 ml vials in a cardboard box.
- 100 ml HDPE vial sealed with nitrile bung and aluminium overseal. 100 ml vial in a cardboard box.
- 100 ml HDPE vial sealed with nitrile bung and aluminium overseal. 12 x 100 ml vials in a cardboard box.
- 100 ml HDPE vial sealed with nitrile bung and aluminium overseal. 12 x 100 ml vials in a polystyrene box.
- 100 ml clear, colourless Type II glass vial, closed with nitrile rubber bung and aluminium overseal. 12 x 100 ml vials in a polystyrene box.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Univet Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Univet Limited
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10990/054/001
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0566/001
Concerned member states:
-
Sweden
Generic of:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
