FDA — authorised 2 January 2003
- Application: BLA103764
- Marketing authorisation holder: NOVARTIS
- Indication: Supplement
- Status: approved
FDA authorised Chrft5 on 2 January 2003
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 2 January 2003.
NOVARTIS holds the US marketing authorisation.