AMBROSPRAY 5%

50MG/G SPR 13ML

SÚKL code 0169041
Name of the product AMBROSPRAY 5%
_MA_MEDICATION_DETAIL_INFO_MED_NAME i AMBROSPRAY 5%
Supplement 50MG/G SPR 13ML
Strenght 50MG/G
Pharmaceutical form Spray
Package 13ML
Route Oromucosal use
Language of the pack Czech
Wrap type
Legal status OTC medicinal products
Active substance AMBROXOL HYDROCHLORIDE (AMBROXOLI HYDROCHLORIDUM)
ATC group R05CB06
ATC group name AMBROXOL

Marketing authorisation information

Registration Number 52/ 130/04-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. 2021
MA Holder CYATHUS Exquirere Pharmaforschungs GmbH, Bisamberg
MA Holder country RAKOUSKO
Actual MA holder GMep Medical Technology GmbH, Düsseldorf
Actual MA holder country NĚMECKO

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