ALENDRONIC ACID AUROBINDO

70MG TBL NOB 50

SÚKL code 0209508
Name of the product ALENDRONIC ACID AUROBINDO 70 MG TABLETY
_MA_MEDICATION_DETAIL_INFO_MED_NAME i ALENDRONIC ACID AUROBINDO
Supplement 70MG TBL NOB 50
Strenght 70MG
Pharmaceutical form Tablet
Package 50
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance SODIUM ALENDRONATE TRIHYDRATE (NATRII ALENDRONAS TRIHYDRICUS)
ATC group M05BA04
ATC group name KYSELINA ALENDRONOVÁ

Marketing authorisation information

Registration Number 87/ 234/14-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 28. 02. 2019
MA Holder Aurobindo Pharma (Malta) Limited, Floriana
MA Holder country MALTA
Actual MA holder Aurovitas, spol. s r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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