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IBANDRONIC ACID AUROBINDO

150MG TBL FLM 3

SÚKL code 0196862
Name of the product IBANDRONIC ACID AUROBINDO 150 MG POTAHOVANÉ TABLETY
_MA_MEDICATION_DETAIL_INFO_MED_NAME i IBANDRONIC ACID AUROBINDO
Supplement 150MG TBL FLM 3
Strenght 150MG
Pharmaceutical form Film-coated tablet
Package 3
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance IBANDRONATE SODIUM MONOHYDRATE (NATRII IBANDRONAS MONOHYDRICUS)
ATC group M05BA06
ATC group name KYSELINA IBANDRONOVÁ

Marketing authorisation information

Registration Number 87/ 110/14-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 30. 04. 2019
MA Holder Aurobindo Pharma (Malta) Limited, Valletta
MA Holder country MALTA
Actual MA holder Aurovitas, spol. s r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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