E-SELENSOL 70/1 mg/ml emulsion for injection for cattle, sheep and pigs
E-SELENSOL 70/1 mg/ml emulsion for injection for cattle, sheep and pigs
Authorised
- ALPHA-TOCOPHEROL
- Sodium selenite
Product identification
Medicine name:
E-SELENSOL 70/1 mg/ml emulsion for injection for cattle, sheep and pigs
E-Selensol, 70/1 mg/ml süsteemulsioon veistele, lammastele ja sigadele
Active substance:
- ALPHA-TOCOPHEROL
- Sodium selenite
Target species:
-
Cattle
-
Pig
-
Sheep
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
ALPHA-TOCOPHEROL70.00milligram(s)1.00millilitre(s)
-
Sodium selenite1.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Meat and offal14dayNot authorised for use in animals producing milk for human consumption.
-
- Pig
-
Meat and offal14day
-
- Sheep
-
Meat and offal30dayNot authorised for use in animals producing milk for human consumption.
-
-
Subcutaneous use
- Cattle
-
Meat and offal14dayNot authorised for use in animals producing milk for human consumption.
-
- Pig
-
Meat and offal14day
-
- Sheep
-
Meat and offal30dayNot authorised for use in animals producing milk for human consumption.
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA12CE99
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Estonia
Available in:
-
Estonia
Package description:
- Type II amber coloured glass vials, with bromobutyl rubber stopper and lacquered aluminium cap. Carton box with 1 vial of 50 ml.
- Type II amber coloured glass vials, with bromobutyl rubber stopper and lacquered aluminium cap. Carton box with 1 vial of 100 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic (abridged application) - art 13(1)
Marketing authorisation holder:
- Labiana Life Sciences S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Labiana Life Sciences S.A.
Responsible authority:
- State Agency Of Medicines
Authorisation number:
- 2285
Date of authorisation status change:
Reference member state:
-
Hungary
Procedure number:
- HU/V/0143/001
Concerned member states:
-
Croatia
-
Cyprus
-
Estonia
-
Greece
-
Latvia
-
Lithuania
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.
Estonian (PDF)
Published on: 1/03/2022
How useful was this page?: