Clamoxyl Prolongatum Vet. injektionsvæske, suspension 150 mg/ml
Clamoxyl Prolongatum Vet. injektionsvæske, suspension 150 mg/ml
Authorised
- Amoxicillin trihydrate
- Amoxicillin trihydrate
Product identification
Medicine name:
Clamoxyl Prolongatum Vet. 150 mg/ml injektionsvæske, suspension
Clamoxyl Prolongatum Vet. injektionsvæske, suspension 150 mg/ml
Active substance:
- Amoxicillin trihydrate
- Amoxicillin trihydrate
Target species:
-
Sheep
-
Cat
-
Cattle
-
Pig
-
Dog
Route of administration:
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Amoxicillin trihydrate176.00/milligram(s)1.00millilitre(s)
-
Amoxicillin trihydrate176.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Sheep
-
Meat and offal52dayMå ikke anvendes til lakterende dyr, der leverer mælk til human konsum.
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Meat and offal52dayMå ikke anvendes til lakterende dyr, der leverer mælk til human konsum.
-
-
Cattle
-
Meat and offal93dayMå ikke anvendes til lakterende dyr, der leverer mælk til human konsum.
-
Meat and offal93dayMå ikke anvendes til lakterende dyr, der leverer mælk til human konsum.
-
-
Pig
-
Meat and offal93dayMå ikke anvendes til lakterende dyr, der leverer mælk til human konsum.
-
Meat and offal93dayMå ikke anvendes til lakterende dyr, der leverer mælk til human konsum.
-
-
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
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Zoetis Animal Health ApS
Marketing authorisation date:
Manufacturing sites for batch release:
- Haupt Pharma Latina S.r.l.
Responsible authority:
- Danish Medicines Agency
Authorisation number:
- 12280
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 (, INJEKTIONSVÆSKE, SUSPENSION 150 MG-ML)
Published on: 29/06/2023
