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EXOROLAK

50MG/ML LAC UGC 1X2,5ML

SÚKL code 0220863
Name of the product EXOROLAK
_MA_MEDICATION_DETAIL_INFO_MED_NAME i EXOROLAK
Supplement 50MG/ML LAC UGC 1X2,5ML
Strenght 50MG/ML
Pharmaceutical form Medicated nail lacquer
Package 1X2,5ML
Route Cutaneous use
Language of the pack Czech
Wrap type Bottle
Legal status na lékařský předpis
Active substance AMOROLFINE HYDROCHLORIDE (AMOROLFINI HYDROCHLORIDUM)
ATC group D01AE16
ATC group name AMOROLFIN

Marketing authorisation information

Registration Number 26/ 010/17-C
Type of MA A mutual recognition procedure (MRP, DCP), where CZ is Concerned member state
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. 01. 2020
MA Holder Laboratoires Gerda, Paris
MA Holder country FRANCIE
Actual MA holder Sandoz s.r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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