🇺🇸 ESCALATED BEACOPP in United States

FDA authorised ESCALATED BEACOPP on 10 November 1983

Marketing authorisations

FDA — authorised 10 November 1983

  • Application: NDA018768
  • Marketing authorisation holder: CORDEN PHARMA
  • Local brand name: VEPESID
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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FDA — authorised 30 December 1986

  • Application: NDA019557
  • Marketing authorisation holder: ONESOURCE SPECIALTY
  • Local brand name: VEPESID
  • Indication: CAPSULE — ORAL
  • Status: approved

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Other Oncology approved in United States

Frequently asked questions

Is ESCALATED BEACOPP approved in United States?

Yes. FDA authorised it on 10 November 1983; FDA authorised it on 30 December 1986.

Who is the marketing authorisation holder for ESCALATED BEACOPP in United States?

CORDEN PHARMA holds the US marketing authorisation.