APO-DICLO

50MG TBL ENT 30

SÚKL code 0107922
Name of the product APO-DICLO 50 MG
_MA_MEDICATION_DETAIL_INFO_MED_NAME i APO-DICLO
Supplement 50MG TBL ENT 30
Strenght 50MG
Pharmaceutical form Gastro-resistant tablet
Package 30
Route Oral use
Language of the pack Czech
Wrap type Tablet container
Legal status na lékařský předpis
Active substance DICLOFENAC SODIUM (DICLOFENACUM NATRICUM)
ATC group M01AB05
ATC group name DIKLOFENAK

Marketing authorisation information

Registration Number 29/1217/94-B/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 31. 08. 2020
MA Holder Apotex Europe B.V., Leiden
MA Holder country NIZOZEMSKO
Actual MA holder Aurovitas, spol. s r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

Back to list