STREPSILS INTENSIVE

This brand name is authorized in Ecuador, Estonia, Ireland, Lithuania, Nigeria, Poland, Romania, South Africa.

Active ingredients

The drug STREPSILS INTENSIVE contains one active pharmaceutical ingredient (API):

1
UNII 5GRO578KLP - FLURBIPROFEN
 

Flurbiprofen is a propionic acid derivative NSAID which acts through inhibition of prostaglandin synthesis. In humans flurbiprofen has potent analgesic, antipyretic and anti-inflammatory properties.
 
Read more about Flurbiprofen

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 STREPSILS INTENSIVE Lozenge MPI, EU: SmPC Health Products Regulatory Authority (IE)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
M01AE09 Flurbiprofen M Musculo-skeletal system → M01 Antiinflammatory and antirheumatic products → M01A Antiinflammatory and antirheumatic products, non-steroids → M01AE Propionic acid derivatives
Discover more medicines within M01AE09
R02AX01 R Respiratory system → R02 Throat preparations → R02A Throat preparations → R02AX Other throat preparations
Discover more medicines within R02AX01

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 5940-MEE-0221, 6439-MEE-0721
EE Ravimiamet 1317394, 1317406, 1317417, 1508655, 1508666, 1508677, 1739763, 1777484, 1810505
LT Valstybinė vaistų kontrolės tarnyba 1027230, 1036286, 1036287, 1089165
NG Registered Drug Product Database A4-9395
Switch country to Nigeria in order to find specific presentations of STREPSILS INTENSIVE
PL Rejestru Produktów Leczniczych 100097114, 100330504, 100385681
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W66075001, W66075002, W66093001, W66093002, W66093003, W66982001, W67603001, W68530001, W68530002, W68530003, W68530004, W68530005, W68531001, W68531002, W68531003, W68531004, W68531005
ZA Health Products Regulatory Authority 35/16/0015

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