Doxatib 500 mg/g powder for use in drinking water for pigs and chickens
Doxatib 500 mg/g powder for use in drinking water for pigs and chickens
Authorised
- Doxycycline hyclate
Product identification
Medicine name:
Doxatib 500 mg/g powder for use in drinking water for pigs and chickens
Doxatib 500 mg/g poeder voor gebruik in drinkwater voor varkens en kippen
Active substance:
- Doxycycline hyclate
Target species:
-
Pig
-
Chicken
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Doxycycline hyclate500.00milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
- Pig
-
Meat and offal4day/
-
- Chicken
-
Meat and offal3dayFollowing a dose rate of 10 mg/kg body weight for 4 days. Do not use within 4 weeks of onset of the laying period.
-
Meat and offal9dayFollowing a dose rate of 20 mg/kg body weight for 4 days. Do not use within 4 weeks of onset of the laying period.
-
Eggno withdrawal periodNot authorised for use in laying birds producing eggs for human consumption.
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Netherlands
Package description:
- Alu quadriplex (PET/Al/PET/PE) bags. Pack sizes of 100 g.
- Alu quadriplex (PET/Al/PET/PE) bags. Pack sizes of 1 kg.
- Alu quadriplex (PET/Al/PET/PE) bags. Pack sizes of 5 kg.
- Alu triplex (PET/Al/PE) bags. Pack sizes of 5 kg.
- Alu triplex (PET/Al/PE) bags.Pack sizes of 1 kg.
- Alu triplex (PET/Al/PE) bags. Pack sizes of 100 g.
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:
- KRKA tovarna zdravil d.d. Novo mesto
Marketing authorisation date:
Manufacturing sites for batch release:
- Tad Pharma GmbH
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 117990
Date of authorisation status change:
Reference member state:
-
Slovenia
Procedure number:
- SI/V/0001/001
Concerned member states:
-
Belgium
-
Bulgaria
-
Croatia
-
Czechia
-
Estonia
-
France
-
Germany
-
Hungary
-
Ireland
-
Latvia
-
Lithuania
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 15/12/2023
Dutch (PDF)
Published on: 26/07/2023
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