CITALOPRAM AUROVITAS
20MG TBL FLM 100
SÚKL code | 0244394 |
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Name of the product | CITALOPRAM AUROVITAS |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | CITALOPRAM AUROVITAS |
Supplement | 20MG TBL FLM 100 |
Strenght | 20MG |
Pharmaceutical form | Film-coated tablet |
Package | 100 |
Route | Oral use |
Language of the pack | Czech |
Wrap type | Blister |
Legal status | na lékařský předpis |
Active substance | CITALOPRAM HYDROBROMIDE (CITALOPRAMI HYDROBROMIDUM) |
ATC group | N06AB04 |
ATC group name | CITALOPRAM |
Marketing authorisation information
Registration Number | 30/ 303/19-C |
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Type of MA | A mutual recognition procedure (MRP, DCP), where CZ is Concerned member state |
MA status | R - active MA/authorised medicinal product |
MA Holder | Aurovitas, spol. s r.o., Praha |
MA Holder country | ČESKÁ REPUBLIKA |