AMOXICILLIN pulvis
AMOXICILLIN pulvis
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
АМОКСИЦИЛИН пулвис
AMOXICILLIN pulvis
Active substance:
- Amoxicillin trihydrate
Target species:
-
Chicken
-
Duck
-
Turkey
-
Pig
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Amoxicillin trihydrate500.00milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for oral solution
Withdrawal period by route of administration:
-
Oral use
- Chicken
-
Meat and offal1dayNot for use in birds witch produce or are intended to produce eggs for human consumption.
-
- Duck
-
Meat and offal9day
-
- Turkey
-
Meat and offal5day
-
- Pig
-
Meat and offal2day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
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:
- Farma Vet OOD
Marketing authorisation date:
Manufacturing sites for batch release:
- Farmavet OOD
Responsible authority:
- Bulgarian Agency For Food Safety
Authorisation number:
- 0022-2900
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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Bulgarian (PDF)
Published on: 12/07/2023
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