Medicinal product name Panadol Extra optizorb 500 mg/65 mg film-coated tablets
Pharmaceutical form Film-coated tablet
Strength 500 mg/65 mg 
Information from the MAH on shortages Not available
predicted availability date: not notified
Legal status OTC OTC
Package leaflet MS Word document 28-03-2019
Summary of product characteristics MS Word document 28-03-2019
ATC code N02BE51 Analgesics

Important notice

Additional information regarding the use for persons aged 75+

If used as "ANALGESICS"
SubstanceClassComment
ParacetamolumASuitable for older persons. Maximum dose in regular use 2-3 g/day. Note paracetamol in OTC drugs and combination products. Overdose is hepatotoxic. Concurrent use with warfarin is possible if INR values are monitored.
CoffeinumASuitable for older persons.

Medicinal products (7)

Availability of medicinal product Wholesalers Package size, content Primary packaging Maximum admissible pharmacy price (€ incl. VAT) Product No. Labelling
 Not available (according to the information provided by wholesalers) currently no information on availability from any wholesaler N8
(500 mg/65 mg)
PVC/Al blister    13-0119-01 Labelling text Labelling text Mar 28, 2019
 Not available (according to the information provided by wholesalers)
predicted availability date: not notified
currently no information on availability from any wholesaler N12
(500 mg/65 mg)
PVC/Al blister    13-0119-02 Labelling text Labelling text Mar 28, 2019
 Not available (according to the information provided by wholesalers) currently no information on availability from any wholesaler N32
(500 mg/65 mg)
PVC/Al blister    13-0119-03 Labelling text Labelling text Mar 28, 2019
 Not available (according to the information provided by wholesalers) currently no information on availability from any wholesaler N14
(500 mg/65 mg)
Carton/PVC box    13-0119-04 Labelling text Labelling text Mar 28, 2019
 Not available (according to the information provided by wholesalers) currently no information on availability from any wholesaler N8
(500 mg/65 mg)
PVC/PET/AL blister    13-0119-05 Labelling text Labelling text Mar 28, 2019
 Not available (according to the information provided by wholesalers) currently no information on availability from any wholesaler N12
(500 mg/65 mg)
PVC/PET/AL blister    13-0119-06 Labelling text Labelling text Mar 28, 2019
 Not available (according to the information provided by wholesalers) currently no information on availability from any wholesaler N32
(500 mg/65 mg)
PVC/PET/AL blister    13-0119-07 Labelling text Labelling text Mar 28, 2019

Registration information

Marketing authorisation No. 13-0119
Date of authorisation May 15, 2013
MA valid until For unlimited time
Marketing authorisation holder, country GlaxoSmithKline Dungarvan Ltd., Ireland