ALENDROGEN
70MG TBL NOB 12
SÚKL code | 0235134 |
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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 |
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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 |