MUCOSOLVAN
15MG PAS MOL 40
SÚKL code | 0223155 |
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Name of the product | MUCOSOLVAN |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | MUCOSOLVAN |
Supplement | 15MG PAS MOL 40 |
Strenght | 15MG |
Pharmaceutical form | Pastille |
Package | 40 |
Route | Oromucosal 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/ 635/09-C |
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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 |