🇺🇸 Cordran in United States

FDA authorised Cordran on 19 March 1963

Marketing authorisations

FDA — authorised 19 March 1963

  • Marketing authorisation holder: AQUA PHARMS
  • Status: approved

FDA — authorised 19 March 1963

  • Application: NDA013790
  • Marketing authorisation holder: INA PHARMS
  • Local brand name: CORDRAN
  • Indication: LOTION — TOPICAL
  • Status: approved

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FDA — authorised 18 October 1965

  • Application: NDA012806
  • Marketing authorisation holder: INA PHARMS
  • Local brand name: CORDRAN
  • Indication: OINTMENT — TOPICAL
  • Status: approved

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FDA — authorised 29 July 1969

  • Application: NDA016455
  • Marketing authorisation holder: ALMIRALL
  • Local brand name: CORDRAN
  • Indication: TAPE — TOPICAL
  • Status: approved

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Cordran in other countries

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

Other Oncology approved in United States

Frequently asked questions

Is Cordran approved in United States?

Yes. FDA authorised it on 19 March 1963; FDA authorised it on 19 March 1963; FDA authorised it on 18 October 1965.

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

AQUA PHARMS holds the US marketing authorisation.