ALLOPURINOL AUROVITAS

300MG TBL NOB 25

SÚKL code 0221875
Name of the product ALLOPURINOL AUROVITAS
_MA_MEDICATION_DETAIL_INFO_MED_NAME i ALLOPURINOL AUROVITAS
Supplement 300MG TBL NOB 25
Strenght 300MG
Pharmaceutical form Tablet
Package 25
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance ALLOPURINOL (ALLOPURINOLUM)
ATC group M04AA01
ATC group name ALOPURINOL

Marketing authorisation information

Registration Number 29/ 145/17-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. 06. 2020
MA Holder Aurovitas Pharma Polska Sp. z o.o., Warszawa
MA Holder country POLSKO
Actual MA holder Aurovitas, spol. s r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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