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PRONTOFLEX 10%

100MG/ML DRM SPR SOL 25ML

SÚKL code 0119940
Name of the product PRONTOFLEX 10%
_MA_MEDICATION_DETAIL_INFO_MED_NAME i PRONTOFLEX 10%
Supplement 100MG/ML DRM SPR SOL 25ML
Strenght 100MG/ML
Pharmaceutical form Cutaneous spray, solution
Package 25ML
Route Cutaneous use
Language of the pack Czech
Wrap type Pressurised container
Legal status na lékařský předpis
Active substance KETOPROFEN (KETOPROFENUM)
ATC group M02AA10
ATC group name KETOPROFEN

Marketing authorisation information

Registration Number 29/ 228/05-C
Type of MA National
MA status B - medicinal product after change, may be placed on the market for the period of 6 months (Placed on the market till) and used until expiration, not later than till the end of validity of the marketing authorisation (Valid till)
Placed on the market till 31. 10. 2020
MA Holder CYATHUS Exquirere Pharmaforschungs GmbH, Bisamberg
MA Holder country RAKOUSKO
Actual MA holder LERAM pharmaceuticals s.r.o., Brno
Actual MA holder country ČESKÁ REPUBLIKA

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