Paracetamolum, Pseudoephedrini hydrochloridum

Medicinal product name Theraflu SN 500 mg/30 mg powder for oral solution
Pharmaceutical form Powder for oral solution
Strength 500 mg/30 mg 
Information from the MAH on shortages No information on expected shortages
Legal status OTC OTC
Package leafletPDF 21-09-2023
Summary of product characteristicsPDF 30-05-2023
Risk minimisation measuresVēstule veselības aprūpes speciālistam Vēstule veselības aprūpes speciālistam
ATC code N02BE51 Analgesics
R05X Cough and cold preparations
Information for Marketing authorisation holdersView

Medicinal products (5)

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 N6
(500 mg/30 mg)
PE terephthalate/ LDPE/Al/LDPE sachet    14-0136-01 Labelling text Labelling text Jan 24, 2019
 Not available (according to the information provided by wholesalers) currently no information on availability from any wholesaler N8
(500 mg/30 mg)
PE terephthalate/ LDPE/Al/LDPE sachet    14-0136-02 Labelling text Labelling text Jan 24, 2019
 Not available (according to the information provided by wholesalers) currently no information on availability from any wholesaler N10
(500 mg/30 mg)
PE terephthalate/ LDPE/Al/LDPE sachet 10.55  14-0136-03 Labelling text Labelling text Jan 24, 2019
 Not available (according to the information provided by wholesalers) currently no information on availability from any wholesaler N12
(500 mg/30 mg)
PE terephthalate/ LDPE/Al/LDPE sachet    14-0136-04 Labelling text Labelling text Jan 24, 2019
 Not available (according to the information provided by wholesalers) currently no information on availability from any wholesaler N14
(500 mg/30 mg)
PE terephthalate/ LDPE/Al/LDPE sachet    14-0136-05 Labelling text Labelling text Jan 24, 2019

Registration information

Marketing authorisation No. 14-0136
Date of authorisation Jun 20, 2014
Marketing authorisation holder, country GlaxoSmithKline Dungarvan Ltd., Ireland