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BELANETTE

0,02MG/3MG TBL FLM 6X21

SÚKL code 0088306
Name of the product BELANETTE 0,02 MG/3 MG POTAHOVANÉ TABLETY
_MA_MEDICATION_DETAIL_INFO_MED_NAME i BELANETTE
Supplement 0,02MG/3MG TBL FLM 6X21
Strenght 0,02MG/3MG
Pharmaceutical form Film-coated tablet
Package 6X21
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance DROSPIRENONE (DROSPIRENONUM)
ETHINYLESTRADIOL BETADEX CLATHRATE (ETHINYLESTRADIOLUM BETADEXUM CLATHRATUM)
ATC group G03AA12
ATC group name DROSPIRENON A ETHINYLESTRADIOL

Marketing authorisation information

Registration Number 17/ 197/06-C
Type of MA A mutual recognition procedure (MRP, DCP), where CZ is Concerned member state
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 30. 06. 2018
MA Holder Bayer Pharma AG, Berlín
MA Holder country NĚMECKO
Actual MA holder Bayer AG, Leverkusen
Actual MA holder country NĚMECKO

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