PALLADONE

1.3 Milligram Capsule

Mundipharma Pharmaceuticals LimitedPA1688/007/001

Main Information

Trade NamePALLADONE
Active SubstancesHYDROMORPHONE HYDROCHLORIDE
Strength1.3 Milligram
Dosage FormCapsule
Licence HolderMundipharma Pharmaceuticals Limited
Licence NumberPA1688/007/001

Group Information

ATC CodeN02AA03 Natural opium alkaloids

Status

Authorised/WithdrawnAuthorised
Licence Issued11/02/2011
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 ReportPDF Version
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Latest Changes to Medicine Info & SPC

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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.