| Code | 2903E | ||||||||||
| MA number | 42/0040/23-S | ||||||||||
| Product Form: | plv ifo 1x500 mg (liek.inj.skl.) | ||||||||||
| MA Status: | R - Valid Marketing Authorisation | ||||||||||
| Type of procedure: | Decentralised | ||||||||||
| MAH, country: | Noridem Enterprises Ltd., Cyprus | ||||||||||
| Therapeutic Class: | 42 - CHEMOTHERAPEUTICA (VRATANE TUBERKULOSTATIK) | ||||||||||
| ATC: |
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| Shelf life: | 30 | ||||||||||
| Container: | glass vial | ||||||||||
| Route of admin.: | Intravenous use |
| Prescription Status: | Medicinal product subject to medical prescription. |
| Legal basis: | Article 10(1) generic application |
| MA issued: | 16.02.2023 |
| Validity: | 16.02.2028 |
| Pediatric indication: | Yes |
| Pediatric posology: | Yes |
| PIL: |
PIL_Aciclovir Noridem_01 2023.pdf
|
| SPC: |
SPC_Aciclovir Noridem plv ifo_10.2025.pdf
|
| Safety feature | Yes |
| Data update: | 09.03.2023 |
