NEOCAPIL

20MG/ML DRM SPR SOL 50ML+APL

SÚKL code 0016901
Name of the product NEOCAPIL
_MA_MEDICATION_DETAIL_INFO_MED_NAME i NEOCAPIL
Supplement 20MG/ML DRM SPR SOL 50ML+APL
Strenght 20MG/ML
Pharmaceutical form Cutaneous spray, solution
Package 50ML+APL
Route Cutaneous use
Language of the pack Czech
Wrap type Bottle
Legal status OTC medicinal products
Active substance MINOXIDIL (MINOXIDILUM)
ATC group D11AX01
ATC group name MINOXIDIL

Marketing authorisation information

Registration Number 46/ 016/92-S/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. 07. 2019
MA Holder Galderma-Spirig Česká a Slovenská republika a. s., Bratislava
MA Holder country SLOVENSKÁ REPUBLIKA
Actual MA holder Galderma International, La Défense
Actual MA holder country FRANCIE

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