Biocillin 1000 mg/g Powder for use in drinking water for chickens, ducks and turkeys
Biocillin 1000 mg/g Powder for use in drinking water for chickens, ducks and turkeys
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Biocillin 1000 mg/g Powder for use in drinking water for chickens, ducks and turkeys
Active substance:
- Amoxicillin trihydrate
Target species:
-
Turkey
-
Chicken
-
Duck
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Amoxicillin trihydrate1000.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Turkey
-
Eggno withdrawal periodNot authorised for use in birds producing eggs for human consumption and within 3 weeks of the start of the laying period.
-
Meat and offal5day
-
-
Chicken
-
Eggno withdrawal periodNot authorised for use in birds producing eggs for human consumption and within 3 weeks of the start of the laying period.
-
Meat and offal1day
-
-
Duck
-
Meat and offal9day
-
Eggno withdrawal periodNot authorised for use in birds producing eggs for human consumption and within 3 weeks of the start of the laying period.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Available in:
-
Greece
Package description:
- (ID1) 250 gram(s): 1 Container (paper; polyethylene; aluminium; low-density polyethylene) with 250 gram(s)
- (ID2) 500 gram(s): 1 Container (paper; polyethylene; aluminium; low-density polyethylene) with 500 gram(s)
- (ID3) 1 kilogram(s): 1 Container (paper; polyethylene; aluminium; low-density polyethylene) with 1 kilogram(s)
- (ID4) 2.5 kilogram(s): 1 Bag (polyethylene; paper; polyethylene; aluminium; polyethylene) with 2.5 kilogram(s)
- (ID5) 5 kilogram(s): 1 Bag (polyethylene; paper; polyethylene; aluminium; polyethylene) with 5 kilogram(s)
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:
- Bela-Pharm GmbH & Co. KG
Marketing authorisation date:
Manufacturing sites for batch release:
- Bela-Pharm GmbH & Co. KG
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 105062/08-11-2021/K-0213501
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0182/001
Concerned member states:
-
Greece
-
Ireland
-
Poland
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
