ANGELIQ

1MG/2MG TBL FLM 1X28

SÚKL code 0018700
Name of the product ANGELIQ
_MA_MEDICATION_DETAIL_INFO_MED_NAME i ANGELIQ
Supplement 1MG/2MG TBL FLM 1X28
Strenght 1MG/2MG
Pharmaceutical form Film-coated tablet
Package 1X28
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance DROSPIRENONE (DROSPIRENONUM)
ESTRADIOL HEMIHYDRATE (ESTRADIOLUM HEMIHYDRICUM)
ATC group G03FA17
ATC group name DROSPIRENON A ESTROGEN

Marketing authorisation information

Registration Number 56/ 102/05-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. 11. 2017
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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