FDA — authorised 29 December 1983
- Application: NDA018366
- Marketing authorisation holder: SAVAGE LABS
- Local brand name: CHYMEX
- Indication: SOLUTION — ORAL
- Status: approved
FDA authorised Chymex on 29 December 1983
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 29 December 1983; FDA has authorised it.
SAVAGE LABS holds the US marketing authorisation.