CLAMOX RTU, 140/35 mg/mL, suspenzija za injekciju za goveda, svinje, pse i mačke
CLAMOX RTU, 140/35 mg/mL, suspenzija za injekciju za goveda, svinje, pse i mačke
Authorised
- Amoxicillin trihydrate
- Clavulanic acid
Product identification
Medicine name:
CLAMOX RTU, 140/35 mg/mL, suspenzija za injekciju za goveda, svinje, pse i mačke
Active substance:
- Amoxicillin trihydrate
- Clavulanic acid
Target species:
-
Dog
-
Cat
-
Cattle
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Amoxicillin trihydrate140.00/milligram(s)1.00millilitre(s)
-
Clavulanic acid35.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal42day
-
Milk60hourU slučaju kombinirane terapije, mlijeko se može koristiti za hranu 60 sati nakon posljednjeg tretmana (nakon 5. mužnje, ako se krave muzu dva puta dnevno).
-
-
Pig
-
Meat and offal31day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CR02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Croatia
Package description:
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
- Available only in Croatian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Crida Pharm S.R.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- Crida Pharm S.R.L.
Responsible authority:
- Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
- UP/I-322-05/22-01/129
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.
Croatian (PDF)
Published on: 31/07/2023
Updated on: 1/08/2023