Code | 80101 | ||||||||||
MA number | EU/1/09/539/001 | ||||||||||
Product Form: | tbl 10x1x15 mg (blister PVC/Al) | ||||||||||
MA Status: | E - Valid centralised marketing authorisation | ||||||||||
Type of procedure: | EU | ||||||||||
MAH, country: | Otsuka Pharmaceutical Netherlands B.V., Netherland | ||||||||||
Therapeutic Class: | 50 - DIURETICA | ||||||||||
ATC: |
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Shelf life: | 48 | ||||||||||
Container: | blister Al/PVC | ||||||||||
Route of admin.: | Oral use |
Prescription Status: | Medicinal product subject to medical prescription. |
Legal basis: | Article 8(3) application - new active substance |
MA issued: | 03.08.2009 |
SmPC + PL: |
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Safety feature | Yes |
Data update: | 30.05.2023 |