Alfacilline 15/15 LA suspensija injekcijām liellopiem, zirgiem, aitām, cūkām, suņiem un kaķiem
Alfacilline 15/15 LA suspensija injekcijām liellopiem, zirgiem, aitām, cūkām, suņiem un kaķiem
Authorised
- Benzylpenicillin procaine
- Benzathine benzylpenicillin
Product identification
Medicine name:
Alfacilline 15/15 LA suspensija injekcijām liellopiem, zirgiem, aitām, cūkām, suņiem un kaķiem
Active substance:
- Benzylpenicillin procaine
- Benzathine benzylpenicillin
Target species:
-
Cattle
-
Horse
-
Sheep
-
Pig
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Benzylpenicillin procaine150.00milligram(s)1.00millilitre(s)
-
Benzathine benzylpenicillin125.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Meat and offal21day
-
Milk6day
-
- Horse
-
Meat and offal21dayNav reģistrēts lietošanai zirgiem, kuru pienu paredzēts izmantot cilvēku uzturā.
-
- Sheep
-
Meat and offal21day
-
Milk6day
-
- Pig
-
Meat and offal21day
-
- Dog
- Cat
-
Subcutaneous use
- Cattle
-
Meat and offal21day
-
Milk6day
-
- Horse
-
Meat and offal21dayNav reģistrēts lietošanai zirgiem, kuru pienu paredzēts izmantot cilvēku uzturā.
-
- Sheep
-
Meat and offal21day
-
Milk6day
-
- Pig
-
Meat and offal21day
-
- Dog
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CE30
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
Package description:
- Available only in Latvian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Alfasan International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Alfasan International B.V.
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/NRP/97/0599
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
This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 7/03/2024
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 7/03/2024
Labelling
This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 7/03/2024
How useful was this page?: