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HYDROMORPHONE HYDROCHLORIDE

20 Mg/Ml Solution for Injection and Concentrate for Infusion

Martindale Pharmaceuticals LtdPA0361/018/001

Main Information

Trade NameHYDROMORPHONE HYDROCHLORIDE
Active SubstancesHYDROMORPHONE HYDROCHLORIDE
Strength20 Mg/Ml
Dosage FormSolution for Injection and Concentrate for Infusion
Licence HolderMartindale Pharmaceuticals Ltd
Licence NumberPA0361/018/001

Group Information

ATC CodeN02AA03 Natural opium alkaloids

Status

Authorised/WithdrawnAuthorised
Licence Issued28/10/2005
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 2 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.