APO-PANTO

40MG TBL ENT 100

SÚKL code 0116436
Name of the product APO-PANTO
_MA_MEDICATION_DETAIL_INFO_MED_NAME i APO-PANTO
Supplement 40MG TBL ENT 100
Strenght 40MG
Pharmaceutical form Gastro-resistant tablet
Package 100
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance PANTOPRAZOLE SODIUM SESQUIHYDRATE (PANTOPRAZOLUM NATRICUM SESQUIHYDRICUM)
ATC group A02BC02
ATC group name PANTOPRAZOL

Marketing authorisation information

Registration Number 09/ 094/08-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. 10. 2020
MA Holder Apotex Europe B.V., Leiden
MA Holder country NIZOZEMSKO
Actual MA holder Aurovitas, spol. s r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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