🇺🇸 Cinobac in United States

FDA authorised Cinobac on 13 June 1980

Marketing authorisations

FDA — authorised 13 June 1980

  • Marketing authorisation holder: LILLY
  • Status: approved

FDA — authorised 13 June 1980

  • Application: NDA018067
  • Marketing authorisation holder: LILLY
  • Local brand name: CINOBAC
  • Indication: CAPSULE — ORAL
  • Status: approved

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FDA — authorised 28 February 1992

  • Application: ANDA073005
  • Marketing authorisation holder: TEVA
  • Local brand name: CINOXACIN
  • Indication: CAPSULE — ORAL
  • Status: approved

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FDA — authorised 28 February 1992

  • Application: ANDA073006
  • Marketing authorisation holder: TEVA
  • Local brand name: CINOXACIN
  • Indication: CAPSULE — ORAL
  • Status: approved

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Cinobac 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 Cinobac approved in United States?

Yes. FDA authorised it on 13 June 1980; FDA authorised it on 13 June 1980; FDA authorised it on 28 February 1992.

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

LILLY holds the US marketing authorisation.