ANALGIN 500 mg/ml injekčný roztok
ANALGIN 500 mg/ml injekčný roztok
Not authorised
- Metamizole sodium
Product identification
Medicine name:
ANALGIN 500 mg/ml injekčný roztok
Active substance:
- Metamizole sodium
Target species:
-
Cattle
-
Horse
-
Dog
Route of administration:
-
Intravenous use
-
Intramuscular use
Product details
Active substance and strength:
-
Metamizole sodium500.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Cattle
-
Meat and offal12day
-
Milk96hour8 milkings
-
-
Horse
-
All relevant tissuesno withdrawal periodDo not use in horses whose meat is intended for human consumption.
-
-
-
Intramuscular use
-
Cattle
-
Meat and offal12day
-
Milk96hour8 milkings
-
-
Horse
-
All relevant tissuesno withdrawal periodDo not use in horses whose meat is intended for human consumption.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN02BB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Slovakia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- BB Pharma a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
- Farmacia Martin a.s.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 07/795/69-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Slovak (PDF)
Published on: 24/11/2021