FDA — authorised 28 December 1982
- Application: NDA018757
- Marketing authorisation holder: MISSION PHARMA
- Local brand name: CALCIBIND
- Indication: POWDER — ORAL
- Status: approved
FDA authorised CELLULOSE SODIUM PHOSPHATE on 28 December 1982
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 28 December 1982; FDA has authorised it.
MISSION PHARMA holds the US marketing authorisation.