Procilline LA Inj. suspension for injection for cattle, sheep, goats, pigs, dogs and cats
Procilline LA Inj. suspension for injection for cattle, sheep, goats, pigs, dogs and cats
Authorised
- Dihydrostreptomycin sulfate
- Benzathine benzylpenicillin
- Benzylpenicillin procaine
Product identification
Medicine name:
Procilline LA Inj. инжекционна суспензия за говеда, овце, кози, свине, кучета и котки
Procilline LA Inj. suspension for injection for cattle, sheep, goats, pigs, dogs and cats
Active substance:
- Dihydrostreptomycin sulfate
- Benzathine benzylpenicillin
- Benzylpenicillin procaine
Target species:
-
Cattle
-
Sheep
-
Goat
-
Pig
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Dihydrostreptomycin sulfate200.00/milligram(s)1.00millilitre(s)
-
Benzathine benzylpenicillin100000.00/international unit(s)1.00millilitre(s)
-
Benzylpenicillin procaine100000.00/international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal49day
-
Milk5day10 издоявания
-
-
Sheep
-
Meat and offal49dayНе се разрешава за употреба при овце и кози, чието мляко е предназначено за човешка консумация
-
-
Goat
-
Meat and offal49dayНе се разрешава за употреба при овце и кози, чието мляко е предназначено за човешка консумация.
-
-
Pig
-
Meat and offal30day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01RA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Package description:
- Available only in Bulgarian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Bibliographical application (stand-alone)
Marketing authorisation holder:
- Kepro B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Kepro B.V.
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-2572
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.
Bulgarian (PDF)
Published on: 26/11/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 26/11/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 26/11/2025