BENZYDAMIN/CETYLPYRIDINIUM CHLORID KRKA
3MG/1MG PAS 32
SÚKL code | 0132305 |
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Name of the product | BENZYDAMIN/CETYLPYRIDINIUM CHLORID KRKA |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | BENZYDAMIN/CETYLPYRIDINIUM CHLORID KRKA |
Supplement | 3MG/1MG PAS 32 |
Strenght | 3MG/1MG |
Pharmaceutical form | Lozenge |
Package | 32 |
Route | Oromucosal use |
Language of the pack | Czech |
Wrap type | Blister |
Legal status | OTC medicinal products |
Active substance |
BENZYDAMINE HYDROCHLORIDE (BENZYDAMINI HYDROCHLORIDUM) CETYLPYRIDINIUM CHLORIDE MONOHYDRATE (CETYLPYRIDINII CHLORIDUM MONOHYDRICUM) |
ATC group | R02AX03 |
ATC group name | BENZYDAMIN |
Marketing authorisation information
Registration Number | 69/ 780/15-C |
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Type of MA | A mutual recognition procedure (MRP, DCP), where CZ is Reference 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. 08. 2020 |
MA Holder | Krka, d.d., Novo mesto, Novo mesto |
MA Holder country | SLOVINSKO |
Actual MA holder | Krka, d.d., Novo mesto, Novo mesto |
Actual MA holder country | SLOVINSKO |