🇺🇸 Psorcon in United States

FDA authorised Psorcon on 14 September 1977

Marketing authorisations

FDA — authorised 14 September 1977

  • Application: NDA017741
  • Marketing authorisation holder: PFIZER
  • Local brand name: FLORONE
  • Indication: CREAM — TOPICAL
  • Status: approved

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FDA — authorised 14 September 1977

  • Marketing authorisation holder: PHARMACIA AND UPJOHN
  • Status: approved

FDA — authorised 1 March 1978

  • Application: NDA017994
  • Marketing authorisation holder: PFIZER
  • Local brand name: PSORCON E
  • Indication: OINTMENT — TOPICAL
  • Status: approved

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FDA — authorised 28 August 1985

  • Application: NDA019260
  • Marketing authorisation holder: PFIZER
  • Local brand name: PSORCON
  • Indication: OINTMENT — TOPICAL
  • Status: approved

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FDA — authorised 20 November 1992

  • Application: NDA020205
  • Marketing authorisation holder: TARO PHARMS NORTH
  • Local brand name: PSORCON
  • Indication: CREAM — TOPICAL
  • Status: approved

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FDA — authorised 30 March 1998

  • Application: ANDA075187
  • Marketing authorisation holder: AVONDALE PHARMS
  • Local brand name: DIFLORASONE DIACETATE
  • Indication: CREAM — TOPICAL
  • Status: approved

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FDA — authorised 27 April 1999

  • Application: ANDA075374
  • Marketing authorisation holder: AVONDALE PHARMS
  • Local brand name: DIFLORASONE DIACETATE
  • Indication: OINTMENT — TOPICAL
  • Status: approved

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FDA — authorised 14 May 1999

  • Application: ANDA075331
  • Marketing authorisation holder: SUN PHARMA CANADA
  • Local brand name: DIFLORASONE DIACETATE
  • Indication: OINTMENT — TOPICAL
  • Status: approved

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FDA — authorised 24 April 2000

  • Application: ANDA075508
  • Marketing authorisation holder: SUN PHARMA CANADA
  • Local brand name: DIFLORASONE DIACETATE
  • Indication: CREAM — TOPICAL
  • Status: approved

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FDA — authorised 20 December 2002

  • Application: ANDA076263
  • Marketing authorisation holder: ANI PHARMS
  • Local brand name: DIFLORASONE DIACETATE
  • Indication: CREAM — TOPICAL
  • Status: approved

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FDA — authorised 24 July 2015

  • Application: ANDA206572
  • Marketing authorisation holder: SCIEGEN PHARMS
  • Local brand name: DIFLORASONE DIACETATE
  • Indication: OINTMENT — TOPICAL
  • Status: approved

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FDA — authorised 27 February 2017

  • Application: ANDA207440
  • Marketing authorisation holder: RISING
  • Local brand name: DIFLORASONE DIACETATE
  • Indication: OINTMENT — TOPICAL
  • Status: approved

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FDA — authorised 12 June 2018

  • Application: ANDA210753
  • Marketing authorisation holder: THE J MOLNER
  • Local brand name: DIFLORASONE DIACETATE
  • Indication: OINTMENT — TOPICAL
  • Status: approved

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Psorcon 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 Psorcon approved in United States?

Yes. FDA authorised it on 14 September 1977; FDA authorised it on 14 September 1977; FDA authorised it on 1 March 1978.

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

PFIZER holds the US marketing authorisation.