Doxycycline Kela, 750 mg/g suukaudse lahuse pulber sigadele
Doxycycline Kela, 750 mg/g suukaudse lahuse pulber sigadele
Authorised
- Doxycycline hyclate
Product identification
Medicine name:
Doxycycline Kela, 750 mg/g suukaudse lahuse pulber sigadele
Active substance:
- Doxycycline hyclate
Target species:
-
Pig
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Doxycycline hyclate932.80/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for oral solution
Withdrawal period by route of administration:
-
Oral use
-
Pig
-
Meat and offal5day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Estonia
Available in:
-
Estonia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Kela Kempisch Laboratorium Kela Laboratoria
Marketing authorisation date:
Manufacturing sites for batch release:
- KELA Kempisch Laboratorium Kela Laboratoria
Responsible authority:
- State Agency Of Medicines
Authorisation number:
- 1551
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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Estonian (PDF)
Published on: 23/05/2024