🇺🇸 ChloraPrep Hi-Lite Orange in United States

FDA authorised ChloraPrep Hi-Lite Orange on 14 July 2000

Marketing authorisation

FDA — authorised 14 July 2000

  • Application: NDA020832
  • Marketing authorisation holder: BECTON DICKINSON CO
  • Local brand name: CHLORAPREP ONE-STEP
  • Indication: SPONGE — TOPICAL
  • Status: approved

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Frequently asked questions

Is ChloraPrep Hi-Lite Orange approved in United States?

Yes. FDA authorised it on 14 July 2000.

Who is the marketing authorisation holder for ChloraPrep Hi-Lite Orange in United States?

BECTON DICKINSON CO holds the US marketing authorisation.