| Code | 9852D | ||||||||||
| MA number | EU/1/21/1620/004 | ||||||||||
| Product Form: | plo por 30x500 mg (vre.PET/Al/PE/laminát) | ||||||||||
| MA Status: | E - Valid centralised marketing authorisation | ||||||||||
| Type of procedure: | EU | ||||||||||
| MAH, country: | Dipharma Arzneimittel GmbH, Germany | ||||||||||
| Therapeutic Class: | 87 - VARIA I | ||||||||||
| ATC: |
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| Shelf life: | 36 | ||||||||||
| Route of admin.: | Oral use |
| Prescription Status: | Medicinal product subject to restricted medical prescription. |
| Legal basis: | Article 10(1) generic application |
| MA issued: | 16.02.2022 |
| Validity: | 16.02.2027 |
| SmPC + PL: |
European Medicines Agency's database
|
| Safety feature | Yes |
| Data update: | 21.02.2023 |
