Octacillin, 800 mg/g powder for oral solution for chickens
- Amoxicillin trihydrate
-
Valid
Product identification
Medicine name:
Octacillin, 800 mg/g powder for oral solution for chickens
Octacillin 800 mg/g poeder voor gebruik in het drinkwater voor kippen
Active substance and strength:
-
Amoxicillin trihydrate
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Authorisation number:
- REG NL 104691
Product identification number:
- 37e2ca96-27a4-4308-ae42-3a6301dfb524
Permanent identification number:
- 600000037122
Product details
Legal status of supply:
This information is not available for this product.
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
- Chicken
-
Meat and offal1day
-
Availability
Package description:
- Sachet 500 g. Sachets consist of a polyester layer on the outside, inside layers of aluminium and polyamide and an inner layer of polyethylene.
- Sachet 250 g. Sachets consist of a white layer on the outside, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene.
- Sachet 500 g. Sachets consist of a white layer on the outside, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene.
- Sachet 250 g. Sachets consist of a polyester layer on the outside, inside layers of aluminium and polyamide and an inner layer of polyethylene.
- Sachet 100 g. Sachets consist of a white layer on the outside, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene.
- Sachet 100 g. Sachets consist of a polyester layer on the outside, inside layers of aluminium and polyamide and an inner layer of polyethylene.
- Sachet 1.0 kg. Sachets consist of a white layer on the outside, inside different transparent layers, a sub-layer of aluminium and an inner layer of polyethylene.
- Sachet 1.0 kg. Sachets consist of a polyester layer on the outside, inside layers of aluminium and polyamide and an inner layer of polyethylene.
Manufacturing sites for batch release:
- Eurovet Animal Health B.V.
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.
Authorisation details
Authorisation status:
-
Valid
Authorisation procedure type:
-
Marketing Authorisation
Procedure number:
- NL/V/0144/001
Date of authorisation status change:
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Authorisation country:
-
Netherlands
Responsible authority:
- Medicines Evaluation Board
Marketing authorisation holder:
- Eurovet Animal Health B.V.
Marketing authorisation issued:
Reference member state:
-
Netherlands
Concerned member states:
-
France
-
Germany
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.
Additional information
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
First published:
Last updated:
First published:
Last updated:
octacilin par.pdf
(PDF)
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