Code | 80604 | ||||||||||
MA number | EU/1/99/123/013 | ||||||||||
Product Form: | tbl flm 6x30x800 mg (fľa. HDPE ) | ||||||||||
MA Status: | E - Valid centralised marketing authorisation | ||||||||||
Type of procedure: | EU | ||||||||||
MAH, country: | Sanofi B.V., Netherland | ||||||||||
Therapeutic Class: | 87 - VARIA I | ||||||||||
ATC: |
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Shelf life: | 36 | ||||||||||
Container: | bottle HDPE | ||||||||||
Route of admin.: | Oral use |
Prescription Status: | Medicinal product subject to medical prescription. |
Legal basis: | Article 8(3) application |
MA issued: | 28.01.2000 |
SmPC + PL: | European Medicines Agency's database |
Safety feature | Yes |
Data update: | 30.06.2021 |