Multimox pulver og solvens til injektionsvæske, opløsning 212 mg/ml
Multimox pulver og solvens til injektionsvæske, opløsning 212 mg/ml
Authorised
- Amoxicillin sodium
Product identification
Medicine name:
Multimox 212 mg/ml pulver og solvens til injektionsvæske, opløsning
Multimox pulver og solvens til injektionsvæske, opløsning 212 mg/ml
Active substance:
- Amoxicillin sodium
Target species:
-
Pig
-
Cattle
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Amoxicillin sodium212.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Powder and solvent for solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
Meat and offal9day
-
-
Cattle
-
Milk3day
-
Meat and offal9day
-
-
-
Intravenous use
-
Cattle
-
Meat and offal5day
-
Milk24hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Denmark
Available in:
-
Denmark
Additional information
Entitlement type:
-
Marketing Authorisation
Marketing authorisation holder:
- Scanvet Animal Health A/S
Marketing authorisation date:
Manufacturing sites for batch release:
- Bela-Pharm GmbH & Co. KG
Responsible authority:
- Danish Medicines Agency
Authorisation number:
- 58257
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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in another language below.
Danish (PDF)
Published on: 4/05/2022