Details
Product Name in the RMS: Duloxetin Actavis
MR Number: SE/H/1467/002
Date of outcome: 09.06.2015
Type of application | |
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Level 1: Level 2: Level 3: Level 4: Level 5: |
Abridged Additional Strength/Form Generic Chemical Substance Prescription Only |
Active Substances |
duloxetine hydrochloride 40 mg |
Form | Gastro-resistant capsule, hard |
MA Holder in the RMS |
Actavis Group PTC ehf Iceland |
RMS | Sweden |
Date of last change | 11.12.2020 |
ATC-Code |
N06AX21 Duloxetine |
CMS Country | Domestic Product Name |
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Poland | Duloxetine Actavis |
Documents | |
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PAR: | https://lakemedelsverket.se/LMF/Lakemedelsinformation/?nplid=20140816000215 (23.10.2015) |
PARSummary: | https://lakemedelsverket.se/LMF/Lakemedelsinformation/?nplid=20140816000215 (23.10.2015) |
FinalSPC: | https://lakemedelsverket.se/LMF/Lakemedelsinformation/?nplid=20140816000215 (08.07.2015) |
FinalPL: | https://lakemedelsverket.se/LMF/Lakemedelsinformation/?nplid=20140816000215 (08.07.2015) |