FDA — authorised 31 October 1949
- Application: NDA006002
- Marketing authorisation holder: SANOFI AVENTIS US
- Local brand name: ARALEN HYDROCHLORIDE
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised CHLOROQUINE HYDROCHLORIDE on 31 October 1949
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 31 October 1949; FDA has authorised it.
SANOFI AVENTIS US holds the US marketing authorisation.