NAPROXEN ARDEZ

550MG TBL FLM 50

SÚKL code 0216203
Name of the product NAPROXEN ARDEZ 550 MG
_MA_MEDICATION_DETAIL_INFO_MED_NAME i NAPROXEN ARDEZ
Supplement 550MG TBL FLM 50
Strenght 550MG
Pharmaceutical form Film-coated tablet
Package 50
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance NAPROXEN SODIUM (NAPROXENUM NATRICUM)
ATC group M01AE02
ATC group name NAPROXEN

Marketing authorisation information

Registration Number 29/ 244/15-C
Type of MA National
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. 01. 2016
MA Holder Krka, d.d., Novo mesto, Novo mesto
MA Holder country SLOVINSKO
Actual MA holder Krka, d.d., Novo mesto, Novo mesto
Actual MA holder country SLOVINSKO

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