ATROPIN BIOTIKA 1 MG
1MG/ML INJ SOL 10X1ML
SÚKL code | 0000394 |
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Name of the product | ATROPIN BIOTIKA 1 MG |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | ATROPIN BIOTIKA 1 MG |
Supplement | 1MG/ML INJ SOL 10X1ML |
Strenght | 1MG/ML |
Pharmaceutical form | Solution for injection |
Package | 10X1ML |
Route | Subcutaneous/intramucsular/intravenous use |
Language of the pack | Czech |
Wrap type | Ampoule |
Legal status | na lékařský předpis |
Active substance | ATROPINE SULFATE MONOHYDRATE (ATROPINI SULFAS MONOHYDRICUS) |
ATC group | A03BA01 |
ATC group name | ATROPIN |
Marketing authorisation information
Registration Number | 53/ 762/92-S/C |
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Type of MA | National |
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. 2020 |
MA Holder | BB Pharma a.s., Praha |
MA Holder country | ČESKÁ REPUBLIKA |
Actual MA holder | BB Pharma a.s., Praha |
Actual MA holder country | ČESKÁ REPUBLIKA |