Selevitan vet. 50 mg/ml+0,6 mg/ml Injektionsvätska, lösning
Selevitan vet. 50 mg/ml+0,6 mg/ml Injektionsvätska, lösning
Authorised
- Sodium selenite
- DL-ALPHA TOCOPHEROL ACETATE
Product identification
Medicine name:
Selevitan vet. 50 mg/ml+0,6 mg/ml Injektionsvätska, lösning
Active substance:
- Sodium selenite
- DL-ALPHA TOCOPHEROL ACETATE
Target species:
-
Sheep
-
Cattle
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Sodium selenite1.32/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
-
Sheep
-
Milk0day
-
Meat and offal2day
-
-
Cattle
-
Milk0day
-
Meat and offal2day
-
-
Pig
-
Meat and offal2day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA12CE99
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Sweden
Available in:
-
Sweden
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Pharmaxim AB
Marketing authorisation date:
Manufacturing sites for batch release:
- Bela-Pharm GmbH & Co. KG
Responsible authority:
- Swedish Medical Products Agency
Authorisation number:
- 9498
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.
Swedish (PDF)
Published on: 10/08/2023
Updated on: 11/08/2023
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Swedish (PDF)
Published on: 10/08/2023
Updated on: 11/08/2023