| Code | 7930C | ||||||||
| MA number | 39/0162/18-S | ||||||||
| Product Form: | tbl mnd 48x500 mg/1000 IU (strip laminát/Al/papier) | ||||||||
| MA Status: | R - Valid Marketing Authorisation | ||||||||
| Type of procedure: | Decentralised | ||||||||
| Therapeutic Class: | 39 - SOLI A IONTY PRO P.O. A PARENT. APLIKÁCIU | ||||||||
| ATC: |
|
||||||||
| Shelf life: | 24 | ||||||||
| Container: | strip laminate/Al/paper | ||||||||
| Route of admin.: | Oral use |
| Prescription Status: | Medicinal product subject to medical prescription. |
| Legal basis: | Article 10a well-established use application |
| MA issued: | 18.05.2018 |
| Validity: | 18.05.2023 |
| MA renewed: | Renewal application submitted |
| Pediatric contraindication: | Yes |
| Pediatric warnings: | Yes |
| SPC: |
SPC_Caltrate D3 500 mg-1000 IU žuvacie tablety_08.2023.pdf
|
| PIL: |
PIL_Caltrate D3 500 mg-1000 IU žuvacie tablety_08.2023.pdf
|
| Safety feature | Yes |
| Data update: | 10.07.2018 |
