FDA — authorised 18 February 1981
- Application: NDA018321
- Marketing authorisation holder: CURIUM
- Local brand name: TECHNESCAN HDP
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised TECHNETIUM TC 99M OXIDRONATE on 18 February 1981
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 18 February 1981; FDA has authorised it.
CURIUM holds the US marketing authorisation.