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RETAFORM

1000MG TBL PRO 56

SÚKL code 0173899
Name of the product RETAFORM
_MA_MEDICATION_DETAIL_INFO_MED_NAME i RETAFORM
Supplement 1000MG TBL PRO 56
Strenght 1000MG
Pharmaceutical form Prolonged-release tablet
Package 56
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance METFORMIN HYDROCHLORIDE (METFORMINI HYDROCHLORIDUM)
ATC group A10BA02
ATC group name METFORMIN

Marketing authorisation information

Registration Number 18/ 875/16-C
Type of MA A mutual recognition procedure (MRP, DCP), where CZ is Reference 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 28. 02. 2022
MA Holder Win Medica S.A., Chalandri
MA Holder country ŘECKO
Actual MA holder Novatin Limited, Mosta
Actual MA holder country MALTA

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