🇺🇸 Kenalog in United States

FDA authorised Kenalog on 4 January 1960

Marketing authorisations

FDA — authorised 4 January 1960

  • Application: NDA012041
  • Marketing authorisation holder: APOTHECON
  • Status: supplemented

FDA — authorised 4 March 1960

  • Application: NDA012097
  • Marketing authorisation holder: DELCOR ASSET CORP
  • Local brand name: KENALOG IN ORABASE
  • Indication: PASTE — DENTAL
  • Status: approved

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FDA — authorised 1 February 1965

  • Application: NDA014901
  • Marketing authorisation holder: APOTHECON
  • Status: supplemented

FDA

  • Status: approved

Other Other approved in United States

Frequently asked questions

Is Kenalog approved in United States?

Yes. FDA authorised it on 4 January 1960; FDA authorised it on 4 March 1960; FDA authorised it on 1 February 1965.

Who is the marketing authorisation holder for Kenalog in United States?

APOTHECON holds the US marketing authorisation.