BENZYDAMIN/CETYLPYRIDINIUM CHLORID KRKA
3MG/1MG PAS 32
| SÚKL code | 0132305 |
|---|---|
| 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 |
|---|---|
| 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 |
cz