Vetalgin vet. 500 mg/ml Injektionsvätska, lösning
Vetalgin vet. 500 mg/ml Injektionsvätska, lösning
Authorised
- Metamizole sodium monohydrate
Product identification
Medicine name:
Vetalgin vet. 500 mg/ml Injektionsvätska, lösning
Active substance:
- Metamizole sodium monohydrate
Target species:
-
Dog
-
Horse
-
Cattle
-
Pig
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Metamizole sodium monohydrate500.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Horse
-
Meat and offal21dayIntravenös behandling 2-3 ggr med 8 timmars intervall med en dos av högst 20-50 mg/kg kroppsvikt:
-
Meat and offal9dayIntravenös behandling som engångsdos med 20-50 mg/kg kroppsvikt
-
-
Cattle
-
Milk4dayIntravenös eller intramuskulär behandling som engångsdos med 20-50 mg/kg kroppsvikt
-
Meat and offal21dayIntravenös eller intramuskulär behandling som engångsdos med 20-50 mg/kg kroppsvikt
-
-
Pig
-
Meat and offal15dayIntravenös eller intramuskulär som engångsdos med 20-50 mg/kg kroppsvikt
-
-
-
Intravenous use
-
Horse
-
Meat and offal9dayIntravenös behandling som engångsdos med 20-50 mg/kg kroppsvikt
-
Meat and offal21dayIntravenös behandling 2-3 ggr med 8 timmars intervall med en dos av högst 20-50 mg/kg kroppsvikt:
-
-
Cattle
-
Milk4dayIntravenös eller intramuskulär behandling som engångsdos med 20-50 mg/kg kroppsvikt
-
Meat and offal21dayIntravenös eller intramuskulär behandling som engångsdos med 20-50 mg/kg kroppsvikt
-
-
Pig
-
Meat and offal15dayIntravenös eller intramuskulär som engångsdos med 20-50 mg/kg kroppsvikt
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN02BB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised 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:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
- Oriola Sweden AB
Responsible authority:
- Swedish Medical Products Agency
Authorisation number:
- 1678
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: 26/04/2022
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: 26/04/2022
