Selevitan, vet. stungulyf, lausn
Selevitan, vet. stungulyf, lausn
Authorised
- Selenide sodium
- DL-ALPHA TOCOPHEROL ACETATE
Product identification
Medicine name:
Selevitan, vet. stungulyf, lausn
Active substance:
- Selenide sodium
- DL-ALPHA TOCOPHEROL ACETATE
Target species:
-
Cattle
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Selenide sodium0.60/milligram(s)1.00millilitre(s)
-
DL-ALPHA TOCOPHEROL ACETATE50.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Meat and offal30day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA12CE99
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Iceland
Package description:
- Available only in Icelandic
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Boehringer Ingelheim Animal Health Denmark A/S
Marketing authorisation date:
Manufacturing sites for batch release:
- Labiana Life Sciences S.A.
Responsible authority:
- Icelandic Medicines Agency
Authorisation number:
- 822959
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.
Icelandic (PDF)
Published on: 14/02/2022
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Icelandic (PDF)
Published on: 14/02/2022
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