REPEN 200,000 IU/ml/250 mg/ml, suspenzija za injiciranje za govedo, ovce, prašiče, pse in mačke
REPEN 200,000 IU/ml/250 mg/ml, suspenzija za injiciranje za govedo, ovce, prašiče, pse in mačke
Authorised
- Dihydrostreptomycin
- Benzylpenicillin
Product identification
Medicine name:
REPEN 200,000 IU/ml/250 mg/ml, suspenzija za injiciranje za govedo, ovce, prašiče, pse in mačke
Active substance:
- Dihydrostreptomycin
- Benzylpenicillin
Target species:
-
Cattle
-
Sheep
-
Pig
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Dihydrostreptomycin250.00/milligram(s)1.00millilitre(s)
-
Benzylpenicillin200000.00/international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal74dayGovedo: Meso in organi: 74 dni
-
Milk108hourGovedo: Mleko: 108 ur
-
-
Sheep
-
Meat and offal74dayOvce: Meso in organi: 74 dni
-
Milk162hourOvce: Mleko: 162 ur
-
-
Pig
-
Meat and offal74dayPrašiči: Meso in organi: 74 dni
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01RA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovenia
Available in:
-
Slovenia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- NP/V/0293/001
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Published on: 7/12/2021