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ALENDROGEN

70MG TBL NOB 12

SÚKL code 0235134
Name of the product ALENDROGEN
_MA_MEDICATION_DETAIL_INFO_MED_NAME i ALENDROGEN
Supplement 70MG TBL NOB 12
Strenght 70MG
Pharmaceutical form Tablet
Package 12
Route Oral use
Language of the pack Czech
Wrap type Tablet container
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/ 120/06-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. 01. 2024
MA Holder Mylan Ireland Limited, Dublin
MA Holder country IRSKO
Actual MA holder VIATRIS LIMITED, Dublin
Actual MA holder country IRSKO

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