Procainii Chloridum 4 % + Adrenalinum 40 mg/ml Solution injectable
Procainii Chloridum 4 % + Adrenalinum 40 mg/ml Solution injectable
Authorised
- EPINEPHRINE BITARTRATE
- Procaine hydrochloride
Product identification
Medicine name:
Procainii Chloridum 4 % + Adrenalinum 40 mg/ml Solution injectable
Procainii Chloridum 4 % + Adrenalinum 40 mg/ml Injektionslösung
Active substance:
- EPINEPHRINE BITARTRATE
- Procaine hydrochloride
Target species:
-
Cattle
-
Sheep
-
Pig
-
Horse
Route of administration:
-
Epidural use
-
Intramuscular use
-
Subcutaneous use
-
Perineural use
Product details
Active substance and strength:
-
EPINEPHRINE BITARTRATE0.04/milligram(s)1.00millilitre(s)
-
Procaine hydrochloride40.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Epidural use
-
Cattle
-
Meat and offal3day
-
-
-
Intramuscular use
-
Cattle
-
Meat and offal3day
-
-
Sheep
-
Meat and offal3day
-
-
Pig
-
Meat and offal3day
-
-
Horse
-
Meat and offal3day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal3day
-
-
Sheep
-
Meat and offal3day
-
-
Pig
-
Meat and offal3day
-
-
Horse
-
Meat and offal3day
-
-
-
Perineural use
-
Cattle
-
Meat and offal3day
-
-
Sheep
-
Meat and offal3day
-
-
Pig
-
Meat and offal3day
-
-
Horse
-
Meat and offal3day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN01BA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Luxembourg
Available in:
-
Luxembourg
Package description:
- Procainii Chloridum 4 % + Adrenalinum 40 mg/ml Solution for injection Vial of 50 ml
- Procainii Chloridum 4 % + Adrenalinum 40 mg/ml Solution for injection Vial of 100 ml
- Procainii Chloridum 4 % + Adrenalinum 40 mg/ml Solution for injection Vial of 250 ml
- Procainii Chloridum 4 % + Adrenalinum 40 mg/ml Solution for injection Vial of 500 ml
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:
- KELA Kempisch Laboratorium Kela Laboratoria
Marketing authorisation date:
Manufacturing sites for batch release:
- KELA Kempisch Laboratorium Kela Laboratoria
Responsible authority:
- Ministry Of Health And Social Security
Authorisation number:
- V 188/18/05/1695
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 4/03/2023
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 4/03/2023
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