🇺🇸 Cefzil® in United States

FDA authorised Cefzil® on 23 December 1991

Marketing authorisations

FDA — authorised 23 December 1991

  • Application: NDA050664
  • Marketing authorisation holder: CORDEN PHARMA
  • Local brand name: CEFZIL
  • Indication: TABLET — ORAL
  • Status: approved

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FDA — authorised 23 December 1991

  • Application: NDA050665
  • Marketing authorisation holder: CORDEN PHARMA
  • Local brand name: CEFZIL
  • Indication: FOR SUSPENSION — ORAL
  • Status: approved

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Frequently asked questions

Is Cefzil® approved in United States?

Yes. FDA authorised it on 23 December 1991; FDA authorised it on 23 December 1991.

Who is the marketing authorisation holder for Cefzil® in United States?

CORDEN PHARMA holds the US marketing authorisation.