🇺🇸 Lidocaine (Zingo) in United States

FDA authorised Lidocaine (Zingo) on 16 August 2007

Marketing authorisation

FDA — authorised 16 August 2007

  • Application: NDA022114
  • Marketing authorisation holder: POWDER PHARMS
  • Local brand name: ZINGO
  • Indication: SYSTEM — INTRADERMAL
  • Status: approved

Read official source →

Other Anesthesia / Pain Management approved in United States

Frequently asked questions

Is Lidocaine (Zingo) approved in United States?

Yes. FDA authorised it on 16 August 2007.

Who is the marketing authorisation holder for Lidocaine (Zingo) in United States?

POWDER PHARMS holds the US marketing authorisation.