🇺🇸 Bovizole in United States

FDA authorised Bovizole on 7 April 1967

Marketing authorisations

FDA — authorised 7 April 1967

  • Status: approved

FDA — authorised 7 April 1967

  • Application: NDA016096
  • Marketing authorisation holder: MERCK SHARP DOHME
  • Local brand name: MINTEZOL
  • Indication: TABLET, CHEWABLE — ORAL
  • Status: approved

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FDA — authorised 21 April 1967

  • Application: NDA016097
  • Marketing authorisation holder: MERCK SHARP DOHME
  • Local brand name: MINTEZOL
  • Indication: SUSPENSION — ORAL
  • Status: approved

Read official source →

Bovizole 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 Bovizole approved in United States?

Yes. FDA authorised it on 7 April 1967; FDA authorised it on 7 April 1967; FDA authorised it on 21 April 1967.

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

Marketing authorisation holder not available in our data.