🇺🇸 Ibuprofen + Paracetamol + Codeine in United States

FDA authorised Ibuprofen + Paracetamol + Codeine on 5 October 1960 · 2 US adverse-event reports

Marketing authorisations

FDA — authorised 5 October 1960

  • Application: NDA012366
  • Marketing authorisation holder: MEDA PHARMS
  • Local brand name: SOMA COMPOUND W/ CODEINE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 9 July 1976

  • Application: ANDA085056
  • Marketing authorisation holder: ORTHO MCNEIL PHARM
  • Local brand name: TYLENOL W/ CODEINE
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 10 May 1978

  • Application: ANDA085638
  • Marketing authorisation holder: SCHERER LABS
  • Local brand name: CODEINE, ASPIRIN, APAP FORMULA NO. 4
  • Indication: CAPSULE — ORAL
  • Status: approved

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FDA — authorised 10 May 1978

  • Application: ANDA085640
  • Marketing authorisation holder: SCHERER LABS
  • Local brand name: CODEINE, ASPIRIN, APAP FORMULA NO. 2
  • Indication: CAPSULE — ORAL
  • Status: approved

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FDA — authorised 10 May 1978

  • Application: ANDA085639
  • Marketing authorisation holder: SCHERER LABS
  • Local brand name: CODEINE, ASPIRIN, APAP FORMULA NO. 3
  • Indication: CAPSULE — ORAL
  • Status: approved

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FDA — authorised 4 January 1985

  • Application: ANDA088896
  • Marketing authorisation holder: WOCKHARDT
  • Local brand name: PROMETHAZINE VC W/ CODEINE
  • Indication: SYRUP — ORAL
  • Status: approved

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FDA — authorised 23 July 1986

  • Application: ANDA089018
  • Marketing authorisation holder: CENCI
  • Local brand name: TRIPROLIDINE AND PSEUDOEPHEDRINE HYDROCHLORIDES W/ CODEINE
  • Indication: SYRUP — ORAL
  • Status: approved

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FDA — authorised 2 March 1987

  • Application: ANDA088870
  • Marketing authorisation holder: HALSEY
  • Local brand name: PHERAZINE VC W/ CODEINE
  • Indication: SYRUP — ORAL
  • Status: approved

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FDA — authorised 30 July 1992

  • Application: NDA020232
  • Marketing authorisation holder: ACTAVIS LABS UT INC
  • Local brand name: FIORICET W/ CODEINE
  • Indication: CAPSULE — ORAL
  • Status: approved

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FDA

  • Application: ANDA085057
  • Marketing authorisation holder: ORTHO MCNEIL PHARM
  • Local brand name: TYLENOL W/ CODEINE
  • Indication: SOLUTION — ORAL
  • Status: approved

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FDA

  • Application: NDA012575
  • Marketing authorisation holder: GLAXOSMITHKLINE
  • Local brand name: ACTIFED W/ CODEINE
  • Indication: SYRUP — ORAL
  • Status: approved

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Safety signals — FAERS

Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.

Most-reported reactions

  1. Cystitis Bacterial — 1 report (50%)
  2. Haematuria — 1 report (50%)

Source database →

Other Pain Management approved in United States

Frequently asked questions

Is Ibuprofen + Paracetamol + Codeine approved in United States?

Yes. FDA authorised it on 5 October 1960; FDA authorised it on 9 July 1976; FDA authorised it on 10 May 1978.

Who is the marketing authorisation holder for Ibuprofen + Paracetamol + Codeine in United States?

MEDA PHARMS holds the US marketing authorisation.