EXODERIL

10MG/ML DRM SOL 1X30ML

SÚKL code 0208317
Name of the product EXODERIL
_MA_MEDICATION_DETAIL_INFO_MED_NAME i EXODERIL
Supplement 10MG/ML DRM SOL 1X30ML
Strenght 10MG/ML
Pharmaceutical form Cutaneous solution
Package 1X30ML
Route Cutaneous use
Language of the pack Czech
Wrap type Dropper container
Legal status OTC medicinal products
Active substance NEFTIFINE HYDROCHLORIDE (NAFTIFINI HYDROCHLORIDUM)
ATC group D01AE22
ATC group name NAFTIFIN

Marketing authorisation information

Registration Number 26/1321/97-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. 03. 2022
MA Holder Sandoz GmbH, Kundl
MA Holder country RAKOUSKO
Actual MA holder Sandoz GmbH, Kundl
Actual MA holder country RAKOUSKO

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