Procaine HCl 2 % Oplossing voor injectie
Procaine HCl 2 % Oplossing voor injectie
Not authorised
- Procaine hydrochloride
Product identification
Medicine name:
Procaine HCl 2 % Oplossing voor injectie
Procaine HCl 2 % Solution injectable
Procaine HCl 2 % Injektionslösung
Active substance:
- Procaine hydrochloride
Target species:
-
Sheep
-
Cattle
-
Pig
-
Dog
-
Horse
-
Cat
Route of administration:
-
Epidural use
-
Subcutaneous use
-
Perineural use
Product details
Active substance and strength:
-
Procaine hydrochloride20.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Epidural use
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Pig
-
Meat and offal0day
-
-
Dog
-
-
Subcutaneous use
-
Horse
-
Meat and offal0day
-
Milk0day
-
-
Cattle
-
Milk0day
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Dog
-
Cat
-
-
Perineural use
-
Dog
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN01BA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Belgium
Package description:
- Procaine HCl 12 Vials with 500 ml of Solution for injection
- Procaine HCl 12 Vials with 250 ml of Solution for injection
- Procaine HCl 12 Vials with 100 ml of Solution for injection
- Procaine HCl 12 Vials with 50 ml of Solution for injection
- Procaine HCl 1 Vial with 500 ml of Solution for injection
- Procaine HCl 1 Vial with 250 ml of Solution for injection
- Procaine HCl 1 Vial with 100 ml of Solution for injection
- Procaine HCl 1 Vial with 50 ml of Solution for injection
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:
- V.M.D.
Marketing authorisation date:
Manufacturing sites for batch release:
- V.M.D.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V104361
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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Package Leaflet
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in another language below.
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