🇺🇸 Sulfurine in United States

FDA authorised Sulfurine on 28 October 1953

Marketing authorisations

FDA — authorised 28 October 1953

  • Status: approved

FDA — authorised 28 October 1953

  • Application: NDA008565
  • Marketing authorisation holder: WYETH AYERST
  • Local brand name: THIOSULFIL
  • Indication: TABLET — ORAL
  • Status: approved

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FDA

  • Application: ANDA080273
  • Marketing authorisation holder: FOREST PHARMS
  • Local brand name: PROKLAR
  • Indication: TABLET — ORAL
  • Status: approved

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FDA

  • Application: ANDA086012
  • Marketing authorisation holder: FOREST PHARMS
  • Local brand name: MICROSUL
  • Indication: TABLET — ORAL
  • Status: approved

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Sulfurine in other countries

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

Other Infectious Disease approved in United States

Frequently asked questions

Is Sulfurine approved in United States?

Yes. FDA authorised it on 28 October 1953; FDA authorised it on 28 October 1953; FDA has authorised it.

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

Marketing authorisation holder not available in our data.