Dewo 100mg/ml šķīdums injekcijām liellopiem, aitām, kazām, cūkām, suņiem, kaķiem
Dewo 100mg/ml šķīdums injekcijām liellopiem, aitām, kazām, cūkām, suņiem, kaķiem
Not authorised
- Levamisole hydrochloride
Product identification
Medicine name:
Dewo 100mg/ml šķīdums injekcijām liellopiem, aitām, kazām, cūkām, suņiem, kaķiem
Active substance:
- Levamisole hydrochloride
Target species:
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Cat
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Cattle
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Sheep
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Goat
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Pig
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Dog
Route of administration:
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Subcutaneous use
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Intramuscular use
Product details
Active substance and strength:
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Levamisole hydrochloride117.90/milligram(s)1.00millilitre(s)
Pharmaceutical form:
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Solution for injection
Withdrawal period by route of administration:
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Subcutaneous use
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Cattle
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Meat and offal8dayNelietot dzīvniekiem, no kuriem iegūst pienu, ko paredzēts izmantot cilvēku uzrturā.
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Sheep
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Meat and offal8dayNelietot dzīvniekiem, no kuriem iegūst pienu, ko paredzēts izmantot cilvēku uzrturā.
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-
Goat
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Meat and offal8dayNelietot dzīvniekiem, no kuriem iegūst pienu, ko paredzēts izmantot cilvēku uzrturā.
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Pig
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Meat and offal8day
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-
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Intramuscular use
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Cattle
-
Meat and offal8dayNelietot dzīvniekiem, no kuriem iegūst pienu, ko paredzēts izmantot cilvēku uzrturā.
-
-
Sheep
-
Meat and offal8dayNelietot dzīvniekiem, no kuriem iegūst pienu, ko paredzēts izmantot cilvēku uzrturā.
-
-
Goat
-
Meat and offal8dayNelietot dzīvniekiem, no kuriem iegūst pienu, ko paredzēts izmantot cilvēku uzrturā.
-
-
Pig
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Meat and offal8day
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-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP52AE01
Legal status of supply:
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Veterinary medicinal product subject to veterinary prescription
Authorisation status:
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Surrendered
Authorised in:
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Latvia
Additional information
Entitlement type:
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Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Bremer Pharma GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Bremer Pharma GmbH
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/NRP/95/0155
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: 25/03/2024
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 25/03/2024
Labelling
This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 25/03/2024
