Suibiofer Se (586 mg + 0,998 mg + 0,00403 mg + 0,03 mg + 0,01 mg + 0,0025 mg + 0,08 mg + 0,4 mg)/ml, surowica świńska do 1 ml Roztwór do wstrzykiwań
Suibiofer Se (586 mg + 0,998 mg + 0,00403 mg + 0,03 mg + 0,01 mg + 0,0025 mg + 0,08 mg + 0,4 mg)/ml, surowica świńska do 1 ml Roztwór do wstrzykiwań
Authorised
- RIBOFLAVIN SODIUM PHOSPHATE
- PORCINE SERUM
- Copper sulphate, anhydrous
- Sodium selenite pentahydrate
- Iron dextran
- Cyanocobalamin
- Nicotinamide
- Pyridoxine hydrochloride
- Thiamine hydrochloride
Product identification
Medicine name:
Suibiofer Se (586 mg + 0,998 mg + 0,00403 mg + 0,03 mg + 0,01 mg + 0,0025 mg + 0,08 mg + 0,4 mg)/ml, surowica świńska do 1 ml Roztwór do wstrzykiwań
Active substance:
- RIBOFLAVIN SODIUM PHOSPHATE
- PORCINE SERUM
- Copper sulphate, anhydrous
- Sodium selenite pentahydrate
- Iron dextran
- Cyanocobalamin
- Nicotinamide
- Pyridoxine hydrochloride
- Thiamine hydrochloride
Target species:
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
RIBOFLAVIN SODIUM PHOSPHATE0.01milligram(s)/millilitre1.00milligram(s)/millilitre
-
PORCINE SERUM1.00millilitre(s)1.00millilitre(s)
-
Copper sulphate, anhydrous0.00milligram(s)1.00millilitre(s)
-
Sodium selenite pentahydrate1.00milligram(s)1.00millilitre(s)
-
Iron dextran586.00milligram(s)1.00millilitre(s)
-
Cyanocobalamin0.08milligram(s)1.00millilitre(s)
-
Nicotinamide0.40milligram(s)1.00millilitre(s)
-
Pyridoxine hydrochloride0.00milligram(s)1.00millilitre(s)
-
Thiamine hydrochloride0.03milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Pig
-
Meat and offal5week
-
-
Subcutaneous use
- Pig
-
Meat and offal5week
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09A
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Fixed combination application (Article 13b of Directive No 2001/82/EC)
Marketing authorisation holder:
- Biowet Drwalew Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Drwalewskie Zakłady Przemysłu Bioweterynaryjnego S.A.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 1121
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.
Polish (PDF)
Published on: 4/02/2022
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 4/02/2022
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 6/02/2023
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