FDA — authorised 16 August 2007
- Application: NDA022114
- Marketing authorisation holder: POWDER PHARMS
- Local brand name: ZINGO
- Indication: SYSTEM — INTRADERMAL
- Status: approved
FDA authorised Lidocaine (Zingo) on 16 August 2007
Yes. FDA authorised it on 16 August 2007.
POWDER PHARMS holds the US marketing authorisation.