Doxylin 100%, powder for use in drinking water/milk for calves and pigs
Doxylin 100%, powder for use in drinking water/milk for calves and pigs
Authorised
- Doxycycline hyclate
Product identification
Medicine name:
Doxylin 100%, powder for use in drinking water/milk for calves and pigs
Doxylin 100% pulveris lietošanai ar dzeramo ūdeni/pienu teļiem un cūkām
Active substance:
- Doxycycline hyclate
Target species:
-
Cattle (calf)
-
Pig
Route of administration:
-
In drinking water/milk use
Product details
Active substance and strength:
-
Doxycycline hyclate1000.00milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water/milk
Withdrawal period by route of administration:
-
In drinking water/milk use
-
Cattle (calf)
-
Meat and offal14day
-
-
Pig
-
Meat and offal8day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
Package description:
- White polypropylene container (bucket) of 5 kg, covered with a polypropylene closure.
- White polypropylene container (bucket) of 2 kg, covered with a polypropylene closure.
- White polypropylene container of 100 grams, covered with a low-density polyethylene closure.
- White polypropylene container (bucket) of 1 kg, covered with a polypropylene closure.
- White polypropylene container of 1 kg, covered with a low-density polyethylene closure.
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:
- Dopharma Research B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Dopharma B.V.
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/MRP/13/0053
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0184/001
Concerned member states:
-
Belgium
-
Denmark
-
Estonia
-
France
-
Germany
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Poland
-
Romania
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 19/03/2024
Latvian (PDF)
Published on: 26/03/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Latvian (PDF)
Published on: 26/03/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Latvian (PDF)
Published on: 26/03/2025
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