🇺🇸 Glutamate in United States

FDA authorised Glutamate on 17 August 1987

Marketing authorisations

FDA — authorised 17 August 1987

  • Application: NDA019398
  • Marketing authorisation holder: OTSUKA ICU MEDCL
  • Indication: Labeling
  • Status: approved

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FDA — authorised 7 September 1988

  • Application: NDA019018
  • Marketing authorisation holder: B BRAUN
  • Indication: Manufacturing (CMC)
  • Status: approved

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FDA — authorised 11 July 1994

  • Application: NDA020015
  • Marketing authorisation holder: OTSUKA ICU MEDCL
  • Indication: Manufacturing (CMC)
  • Status: approved

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FDA — authorised 28 February 2001

  • Application: ANDA020512
  • Marketing authorisation holder: BAXTER HLTHCARE
  • Indication: Labeling
  • Status: approved

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FDA — authorised 12 April 2016

  • Application: NDA200656
  • Marketing authorisation holder: FRESENIUS KABI USA
  • Indication: Labeling
  • Status: approved

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FDA

  • Status: approved

Glutamate in other countries

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

Other Neuroscience approved in United States

Frequently asked questions

Is Glutamate approved in United States?

Yes. FDA authorised it on 17 August 1987; FDA authorised it on 7 September 1988; FDA authorised it on 11 July 1994.

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

OTSUKA ICU MEDCL holds the US marketing authorisation.