🇺🇸 Norepinephrine Bitartrate In 5% Dextrose in United States

FDA authorised Norepinephrine Bitartrate In 5% Dextrose on 13 July 1950

Marketing authorisations

FDA — authorised 13 July 1950

  • Marketing authorisation holder: HOSPIRA
  • Status: approved

FDA — authorised 31 August 2015

  • Application: ANDA040455
  • Marketing authorisation holder: MEITHEAL
  • Indication: Manufacturing (CMC)
  • Status: approved

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FDA — authorised 4 October 2018

  • Application: ANDA211242
  • Marketing authorisation holder: MYLAN LABS LTD
  • Status: approved

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FDA — authorised 17 December 2018

  • Application: ANDA210839
  • Marketing authorisation holder: AMNEAL
  • Status: approved

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FDA — authorised 15 January 2021

  • Application: NDA214313
  • Marketing authorisation holder: BAXTER HLTHCARE CORP
  • Local brand name: NOREPINEPHRINE BITARTRATE IN 5% DEXTROSE
  • Indication: SOLUTION — INTRAVENOUS
  • Status: approved

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FDA — authorised 6 October 2022

  • Application: NDA214628
  • Marketing authorisation holder: LONG GROVE PHARMS
  • Indication: Type 5 - New Formulation or New Manufacturer
  • Status: approved

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FDA — authorised 15 September 2023

  • Application: ANDA217575
  • Marketing authorisation holder: CAPLIN
  • Status: approved

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FDA — authorised 11 August 2025

  • Application: ANDA219692
  • Marketing authorisation holder: SAGENT
  • Local brand name: NOREPINEPHRINE BITARTRATE IN 5% DEXTROSE
  • Indication: SOLUTION — INTRAVENOUS
  • Status: approved

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FDA — authorised 26 March 2026

  • Application: ANDA220483
  • Marketing authorisation holder: SAGENT
  • Local brand name: NOREPINEPHRINE BITARTRATE IN 5% DEXTROSE
  • Indication: SOLUTION — INTRAVENOUS
  • Status: approved

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Norepinephrine Bitartrate In 5% Dextrose in other countries

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

Other Cardiovascular approved in United States

Frequently asked questions

Is Norepinephrine Bitartrate In 5% Dextrose approved in United States?

Yes. FDA authorised it on 13 July 1950; FDA authorised it on 31 August 2015; FDA authorised it on 4 October 2018.

Who is the marketing authorisation holder for Norepinephrine Bitartrate In 5% Dextrose in United States?

HOSPIRA holds the US marketing authorisation.