MUCOSOLVAN

30MG TBL NOB 20

SÚKL code 0223157
Name of the product MUCOSOLVAN
_MA_MEDICATION_DETAIL_INFO_MED_NAME i MUCOSOLVAN
Supplement 30MG TBL NOB 20
Strenght 30MG
Pharmaceutical form Tablet
Package 20
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status OTC medicinal products
Active substance AMBROXOL HYDROCHLORIDE (AMBROXOLI HYDROCHLORIDUM)
ATC group R05CB06
ATC group name AMBROXOL

Marketing authorisation information

Registration Number 52/ 122/81-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. 12. 2021
MA Holder sanofi-aventis, s.r.o., Praha
MA Holder country ČESKÁ REPUBLIKA
Actual MA holder Opella Healthcare Czech s.r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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