Biocillin 1000 mg/g Powder for Use in Drinking Water for Chickens, Ducks and Turkeys

Authorised

Amoxicillin trihydrate

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Product identification

Medicine name:

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

Active substance:

Amoxicillin trihydrate

Target species:

Turkey
Chicken
Duck

Route of administration:

In drinking water use

Product details

Active substance and strength:

Amoxicillin trihydrate

1000.00

milligram(s)

/

1.00

gram(s)

Pharmaceutical form:

Oral powder

Withdrawal period by route of administration:

In drinking water use
- Turkey
  - Egg
    
    no withdrawal period
    
    Not authorised for use in birds producing eggs for human consumption and within 3 weeks of the start of the laying period.
  - Meat and offal
    
    5
    
    day
- Chicken
  - Egg
    
    no withdrawal period
    
    Not authorised for use in birds producing eggs for human consumption and within 3 weeks of the start of the laying period.
  - Meat and offal
    
    1
    
    day
- Duck
  - Meat and offal
    
    9
    
    day
  - Egg
    
    no withdrawal period
    
    Not 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:

United Kingdom (Northern Ireland)

Available in:

United Kingdom (Northern Ireland)

Package description:

(ID5) 5 kilogram(s): unspecified outer container with 1 Sachet (PolyEthylene; Paper; PolyEthylene; Aluminium; PolyEthylene) with 5 kilogram(s)
(ID4) 2.5 kilogram(s): unspecified outer container with 1 Sachet (PolyEthylene; Paper; PolyEthylene; Aluminium; PolyEthylene) with 2.5 kilogram(s)
(ID3) 1 kilogram(s): unspecified outer container with 1 Container (Paper; PolyEthylene; Aluminium; Low Density PolyEthylene) with 1 kilogram(s)
(ID2) 500 gram(s): unspecified outer container with 1 Container (Paper; PolyEthylene; Aluminium; Low Density PolyEthylene) with 500 gram(s)
(ID1) 250 gram(s): unspecified outer container with 1 Container (Paper; PolyEthylene; Aluminium; Low Density PolyEthylene) with 250 gram(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:

22/06/2016

Manufacturing sites for batch release:

Bela-Pharm GmbH & Co. KG

Responsible authority:

The Veterinary Medicines Directorate

Authorisation number:

Vm 41816/4001

Date of authorisation status change:

9/06/2023

Reference member state:

Germany

Procedure number:

DE/V/0182/001

Concerned member states:

Greece
Ireland
Poland
Slovakia
United Kingdom (Northern Ireland)

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

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