Optidox Vet. pulver til anvendelse i drikkevand 500 mg/g
Optidox Vet. pulver til anvendelse i drikkevand 500 mg/g
Authorised
- Doxycycline hyclate
- Doxycycline hyclate
- Doxycycline hyclate
- Doxycycline hyclate
Product identification
Medicine name:
Optidox Vet. 500 mg/g pulver til anvendelse i drikkevand
Optidox Vet. pulver til anvendelse i drikkevand 500 mg/g
Active substance:
- Doxycycline hyclate
- Doxycycline hyclate
- Doxycycline hyclate
- Doxycycline hyclate
Target species:
-
Pig
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Doxycycline hyclate500.00/milligram(s)1.00gram(s)
-
Doxycycline hyclate500.00/milligram(s)1.00gram(s)
-
Doxycycline hyclate500.00/milligram(s)1.00gram(s)
-
Doxycycline hyclate500.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
Oral use
-
Pig
-
Meat and offal4day
-
Meat and offal4day
-
Meat and offal4day
-
Meat and offal4day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Denmark
Additional information
Entitlement type:
-
Marketing Authorisation
Marketing authorisation holder:
- Eurovet Animal Health B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Eurovet Animal Health B.V.
Responsible authority:
- Danish Medicines Agency
Authorisation number:
- 50695
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Danish (, PULVER TIL ANVENDELSE I DRIKKEVAND 500 MG-G)
Published on: 27/01/2025