AMOKSIKLAV 625 MG

500MG/125MG TBL FLM 21

SÚKL code 0085525
Name of the product AMOKSIKLAV 625 MG
_MA_MEDICATION_DETAIL_INFO_MED_NAME i AMOKSIKLAV 625 MG
Supplement 500MG/125MG TBL FLM 21
Strenght 500MG/125MG
Pharmaceutical form Film-coated tablet
Package 21
Route Oral use
Language of the pack Czech
Wrap type Blister
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/ 265/92-B/C
Type of MA National
MA status R - active MA/authorised medicinal product
MA Holder Lek Pharmaceuticals d.d., Ljubljana
MA Holder country SLOVINSKO

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