🇺🇸 Eurax in United States

FDA authorised Eurax on 6 July 1949

Marketing authorisations

FDA — authorised 6 July 1949

  • Marketing authorisation holder: RANBAXY
  • Status: approved

FDA — authorised 6 July 1949

  • Application: NDA006927
  • Marketing authorisation holder: JOURNEY
  • Local brand name: EURAX
  • Indication: CREAM — TOPICAL
  • Status: approved

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FDA — authorised 29 April 1955

  • Application: NDA009112
  • Marketing authorisation holder: JOURNEY
  • Local brand name: EURAX
  • Indication: LOTION — TOPICAL
  • Status: approved

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FDA — authorised 16 December 1981

  • Application: ANDA087204
  • Marketing authorisation holder: LEGACY PHARMA
  • Local brand name: CROTAN
  • Indication: LOTION — TOPICAL
  • Status: approved

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Eurax in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Other Dermatology approved in United States

Frequently asked questions

Is Eurax approved in United States?

Yes. FDA authorised it on 6 July 1949; FDA authorised it on 6 July 1949; FDA authorised it on 29 April 1955.

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

RANBAXY holds the US marketing authorisation.