🇺🇸 Dry Ice in United States

FDA authorised Dry Ice on 5 July 2013

Marketing authorisations

FDA — authorised 5 July 2013

  • Application: NDA205815
  • Marketing authorisation holder: LINDE MERCHANT PRODUCTIONS INC
  • Indication: Medical Gas
  • Status: approved

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FDA — authorised 20 July 2013

  • Application: NDA205846
  • Marketing authorisation holder: AIRGAS CARBONIC INC
  • Indication: Medical Gas
  • Status: approved

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FDA — authorised 18 July 2020

  • Application: NDA215007
  • Marketing authorisation holder: NEXAIR LLC
  • Status: approved

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FDA — authorised 25 February 2022

  • Application: NDA217082
  • Marketing authorisation holder: CONTINENTAL CARBONIC PRODUCTS, INC.
  • Status: approved

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FDA — authorised 10 August 2024

  • Application: NDA219779
  • Marketing authorisation holder: CENTRAL WELDING SUPPLY
  • Status: approved

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Dry Ice in other countries

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

Other Other approved in United States

Frequently asked questions

Is Dry Ice approved in United States?

Yes. FDA authorised it on 5 July 2013; FDA authorised it on 20 July 2013; FDA authorised it on 18 July 2020.

Who is the marketing authorisation holder for Dry Ice in United States?

LINDE MERCHANT PRODUCTIONS INC holds the US marketing authorisation.