DIAREG

1000MG TBL FLM 70 II

SÚKL code 0225522
Name of the product DIAREG
_MA_MEDICATION_DETAIL_INFO_MED_NAME i DIAREG
Supplement 1000MG TBL FLM 70 II
Strenght 1000MG
Pharmaceutical form Film-coated tablet
Package 70 II
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/ 162/14-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 31. 10. 2018
MA Holder Aurovitas Pharma Polska Sp. z o.o., Warszawa
MA Holder country POLSKO
Actual MA holder Aurovitas Pharma Polska Sp. z o.o., Warszawa
Actual MA holder country POLSKO

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