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AVODART

0,5MG CPS MOL 10

SÚKL code 0016902
Name of the product AVODART
_MA_MEDICATION_DETAIL_INFO_MED_NAME i AVODART
Supplement 0,5MG CPS MOL 10
Strenght 0,5MG
Pharmaceutical form Capsule, soft
Package 10
Route Oral use
Wrap type Blister
Legal status na lékařský předpis
Active substance DUTASTERIDE (DUTASTERIDUM)
ATC group G04CB02
ATC group name DUTASTERID

Marketing authorisation information

Registration Number 87/ 287/03-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 31. 07. 2019
MA Holder Glaxo Group Limited, Brentford
MA Holder country VELKÁ BRITÁNIE
Actual MA holder GlaxoSmithKline (Ireland) Limited, Dublin
Actual MA holder country IRSKO

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