KETALAR

50 Mg/Ml Solution for Inj/Inf

Pfizer Healthcare IrelandPA0822/013/002

Main Information

Trade NameKETALAR
Active SubstancesKETAMINE HYDROCHLORIDE
Strength50 Mg/Ml
Dosage FormSolution for Inj/Inf
Licence HolderPfizer Healthcare Ireland
Licence NumberPA0822/013/002

Group Information

ATC CodeN01AX03 Other general anesthetics

Status

Authorised/WithdrawnAuthorised
Licence Issued01/04/2000
Supply StatusSupply through pharmacies only
Dispensing StatusProduct subject to prescription which may not be renewed (A)
Marketing StatusMarketed
Promotion StatusPromotion to Healthcare Professionals only
Conditions of LicenceThis product contains a substance listed in Schedule 3 to the Misuse of Drugs Regulations 1988 (S.I. No. 328 of 1988), as amended.

Documents

Summary of Product CharacteristicsPDF Version
Package LeafletPDF Version
Public Assessment ReportNo document available
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Please note changes to the medicine information and summary of product characteristics are only available from the 19/05/2015 onwards. Changes made before this date aren't available online.