AMOKSIKLAV 457 MG/5 ML
400MG/5ML+57MG/5ML POR PLV SUS 140ML
SÚKL code | 0099367 |
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Name of the product | AMOKSIKLAV 457 MG/5 ML |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | AMOKSIKLAV 457 MG/5 ML |
Supplement | 400MG/5ML+57MG/5ML POR PLV SUS 140ML |
Strenght | 400MG/5ML+57MG/5ML |
Pharmaceutical form | Powder for oral suspension |
Package | 140ML |
Route | Oral use |
Language of the pack | Czech |
Wrap type | Bottle |
Legal status | na lékařský předpis |
Active substance |
POTASSIUM CLAVULANATE (KALII CLAVULANAS) AMOXICILLIN TRIHYDRATE (AMOXICILLINUM TRIHYDRICUM) |
ATC group | J01CR02 |
ATC group name | AMOXICILIN A INHIBITOR BETA-LAKTAMASY |
Marketing authorisation information
Registration Number | 15/ 387/05-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. 10. 2021 |
MA Holder | Lek Pharmaceuticals d.d., Ljubljana |
MA Holder country | SLOVINSKO |
Actual MA holder | Lek Pharmaceuticals d.d., Ljubljana |
Actual MA holder country | SLOVINSKO |