BELAMOX, milteliai ir tirpiklis injekciniam tirpalui
BELAMOX, milteliai ir tirpiklis injekciniam tirpalui
Authorised
- Amoxicillin sodium
Product identification
Medicine name:
BELAMOX, milteliai ir tirpiklis injekciniam tirpalui
Active substance:
- Amoxicillin sodium
Target species:
-
Cattle (calf)
-
Horse
-
Pig
-
Cattle
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Amoxicillin sodium5.30gram(s)1.00Vial
Pharmaceutical form:
-
Powder and solvent for solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle (calf)
-
Meat9day
-
- Horse
-
Meat16day
-
- Pig
-
Meat9day
-
- Cattle
-
Meat9day
-
Milk3day
-
-
Intravenous use
- Cattle
-
Meat5day
-
Milk24hour
-
- Cattle (calf)
-
Meat5day
-
- Horse
-
Meat5day
-
-
Subcutaneous use
- Cattle
-
Meat9day
-
Milk3day
-
- Cattle (calf)
-
Meat9day
-
- Pig
-
Meat9day
-
- Horse
-
Meat16day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Package description:
- Available only in Lithuanian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Bela-Pharm GmbH & Co. KG
Marketing authorisation date:
Manufacturing sites for batch release:
- Bela-Pharm GmbH & Co. KG
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/07/1761/001
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
RV1761.pdf
Lithuanian (PDF)
Download Published on: 3/08/2022
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