🇺🇸 Oncovin in United States

FDA authorised Oncovin on 10 July 1963

Marketing authorisations

FDA — authorised 10 July 1963

  • Application: NDA014103
  • Marketing authorisation holder: LILLY
  • Local brand name: ONCOVIN
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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FDA — authorised 17 July 1987

  • Application: ANDA071426
  • Marketing authorisation holder: TEVA PARENTERAL
  • Local brand name: VINCASAR PFS
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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FDA — authorised 19 April 1988

  • Application: ANDA071484
  • Marketing authorisation holder: HOSPIRA
  • Local brand name: VINCRISTINE SULFATE PFS
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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FDA — authorised 1 September 1999

  • Application: ANDA075493
  • Marketing authorisation holder: TEVA PHARMS USA
  • Local brand name: VINCRISTINE SULFATE PFS
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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FDA — authorised 20 December 2002

  • Application: ANDA076296
  • Marketing authorisation holder: FRESENIUS KABI USA
  • Local brand name: VINCRISTINE SULFATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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FDA — authorised 28 October 2003

  • Application: ANDA076401
  • Marketing authorisation holder: FRESENIUS KABI USA
  • Local brand name: VINCRISTINE SULFATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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FDA — authorised 9 August 2012

  • Application: NDA202497
  • Marketing authorisation holder: ACROTECH
  • Local brand name: MARQIBO KIT
  • Indication: INJECTABLE, LIPOSOMAL — INTRAVENOUS
  • Status: approved

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FDA

  • Application: ANDA070777
  • Marketing authorisation holder: QUAD PHARMS
  • Local brand name: VINCRISTINE SULFATE
  • Indication: Injectable — Injection
  • Status: approved

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FDA

  • Application: ANDA070778
  • Marketing authorisation holder: QUAD PHARMS
  • Local brand name: VINCRISTINE SULFATE
  • Indication: Injectable — Injection
  • Status: approved

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FDA

  • Application: ANDA071937
  • Marketing authorisation holder: QUAD PHARMS
  • Local brand name: VINCRISTINE SULFATE
  • Indication: Injectable — Injection
  • Status: approved

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FDA

  • Application: ANDA070411
  • Marketing authorisation holder: ABRAXIS PHARM
  • Local brand name: VINCRISTINE SULFATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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FDA

  • Application: ANDA071559
  • Marketing authorisation holder: HOSPIRA
  • Local brand name: VINCRISTINE SULFATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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FDA

  • Application: ANDA071560
  • Marketing authorisation holder: HOSPIRA
  • Local brand name: VINCRISTINE SULFATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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FDA

  • Application: ANDA071561
  • Marketing authorisation holder: HOSPIRA
  • Local brand name: VINCRISTINE SULFATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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FDA

  • Application: ANDA070873
  • Marketing authorisation holder: ABIC
  • Local brand name: VINCRISTINE SULFATE
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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Oncovin 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 Oncovin approved in United States?

Yes. FDA authorised it on 10 July 1963; FDA authorised it on 17 July 1987; FDA authorised it on 19 April 1988.

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

LILLY holds the US marketing authorisation.