🇺🇸 Triiodothyronine in United States

FDA authorised Triiodothyronine on 8 May 1956

Marketing authorisations

FDA — authorised 8 May 1956

  • Application: NDA010379
  • Marketing authorisation holder: KING PHARMS
  • Local brand name: CYTOMEL
  • Indication: TABLET — ORAL
  • Status: approved

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FDA

  • Status: approved

Other Oncology approved in United States

Frequently asked questions

Is Triiodothyronine approved in United States?

Yes. FDA authorised it on 8 May 1956; FDA has authorised it.

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

KING PHARMS holds the US marketing authorisation.