AMOKSIKLAV 625 MG
500MG/125MG TBL FLM 21
| SÚKL code | 0254953 |
|---|---|
| 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 | Strip |
| 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 |
cz