| Code | 2483E | ||||||||||
| MA number | EU/1/22/1691/001 | ||||||||||
| Product Form: | sol inj 1x0,23 ml/2,3 mg (liek.inj.skl.) | ||||||||||
| MA Status: | E - Valid centralised marketing authorisation | ||||||||||
| Type of procedure: | EU | ||||||||||
| MAH, country: | STADA Arzneimittel AG, Germany | ||||||||||
| Therapeutic Class: | 64 - OPHTHALMOLOGICA | ||||||||||
| ATC: |
|
||||||||||
| Shelf life: | 36 | ||||||||||
| Container: | glass vial | ||||||||||
| Route of admin.: | Intravitreal use |
| Prescription Status: | Medicinal product subject to restricted medical prescription. |
| Legal basis: | Article 10(4) similar biological application |
| MA issued: | 09.11.2022 |
| Validity: | 09.11.2027 |
| SmPC + PL: |
European Medicines Agency's database
|
| Dokument: |
Ranibizumab_Prirucka pre pacientov.pdf
|
| Safety feature | Yes |
| Data update: | 06.12.2022 |
