Laksans 500 g peroralni prašek
Laksans 500 g peroralni prašek
Not authorised
- Magnesium sulfate heptahydrate
Product identification
Medicine name:
Laksans 500 g peroralni prašek
Active substance:
- Magnesium sulfate heptahydrate
Target species:
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Cattle
-
Horse
-
Sheep
-
Goat
-
Pig
Route of administration:
-
In drinking water/milk use
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In-feed use
Product details
Active substance and strength:
-
Magnesium sulfate heptahydrate500.00/gram(s)1.00Bag
Pharmaceutical form:
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Oral powder
Withdrawal period by route of administration:
-
In drinking water/milk use
-
Cattle
-
Meat and offal, milk0dayMeso in organi: nič dni. Mleko: nič dni.
-
-
Horse
-
Meat and offal, milk0day
-
-
Sheep
-
Meat and offal, milk0day
-
-
Goat
-
Meat and offal, milk0day
-
-
Pig
-
Meat and offal0day
-
-
-
In-feed use
-
Cattle
-
Meat and offal, milk0day
-
-
Horse
-
Meat and offal, milk0day
-
-
Sheep
-
Meat and offal, milk0day
-
-
Goat
-
Meat and offal, milk0day
-
-
Pig
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA06AD04
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Slovenia
Package description:
- Available only in Slovenian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- GENERA SI podjetje za zastopanje in trgovino d.o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Genera d.d.
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- NP/V/0184/001
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.
Slovenian (PDF)
Published on: 29/11/2021
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it
in another language below.
Slovenian (PDF)
Published on: 29/11/2021