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AMOKSIKLAV 457 MG/5 ML

400MG/5ML+57MG/5ML POR PLV SUS 70ML

SÚKL code 0099366
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 70ML
Strenght 400MG/5ML+57MG/5ML
Pharmaceutical form Powder for oral suspension
Package 70ML
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
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

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