PULMICORT

0,5MG/ML SUS NEB 20X2ML

SÚKL code 0013033
Name of the product PULMICORT
_MA_MEDICATION_DETAIL_INFO_MED_NAME i PULMICORT
Supplement 0,5MG/ML SUS NEB 20X2ML
Strenght 0,5MG/ML
Pharmaceutical form Nebuliser suspension
Package 20X2ML
Route Inhalation use
Language of the pack Czech
Wrap type Ampoule
Legal status na lékařský předpis
Active substance BUDESONIDE (BUDESONIDUM)
ATC group R03BA02
ATC group name BUDESONID

Marketing authorisation information

Registration Number 14/ 684/97-C
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 28. 02. 2019
MA Holder AstraZeneca UK Limited, Cambridge
MA Holder country VELKÁ BRITÁNIE
Actual MA holder AstraZeneca AB, Södertälje
Actual MA holder country ŠVÉDSKO

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