AMBROXOL AL RETARD
75MG CPS PRO 20
SÚKL code | 0043947 |
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Name of the product | AMBROXOL AL RETARD |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | AMBROXOL AL RETARD |
Supplement | 75MG CPS PRO 20 |
Strenght | 75MG |
Pharmaceutical form | Prolonged-release capsule, hard |
Package | 20 |
Route | Oral use |
Language of the pack | Czech |
Wrap type | Blister |
Legal status | OTC medicinal products |
Active substance | AMBROXOL HYDROCHLORIDE (AMBROXOLI HYDROCHLORIDUM) |
ATC group | R05CB06 |
ATC group name | AMBROXOL |
Marketing authorisation information
Registration Number | 52/ 266/95-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 | 31. 08. 2021 |
MA Holder | Aliud Pharma GmbH, Laichingen |
MA Holder country | NĚMECKO |
Actual MA holder | STADA Arzneimittel AG, Bad Vilbel |
Actual MA holder country | NĚMECKO |