AKARBOZA MYLAN
100MG TBL NOB 180
SÚKL code | 0124066 |
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Name of the product | AKARBOZA MYLAN |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | AKARBOZA MYLAN |
Supplement | 100MG TBL NOB 180 |
Strenght | 100MG |
Pharmaceutical form | Tablet |
Package | 180 |
Route | Oral use |
Language of the pack | Czech |
Wrap type | Blister |
Legal status | na lékařský předpis |
Active substance | ACARBOSE (ACARBOSUM) |
ATC group | A10BF01 |
ATC group name | AKARBOSA |
Marketing authorisation information
Registration Number | 18/ 613/08-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. 2019 |
MA Holder | Generics [UK] Limited, Potters Bar |
MA Holder country | VELKÁ BRITÁNIE |
Actual MA holder | Mylan Ireland Limited, Dublin |
Actual MA holder country | IRSKO |