🇺🇸 Prednisolone 1% in United States

FDA authorised Prednisolone 1% on 30 May 1973

Marketing authorisations

FDA — authorised 30 May 1973

  • Application: NDA017011
  • Marketing authorisation holder: ABBVIE
  • Local brand name: PRED FORTE
  • Indication: SUSPENSION/DROPS — OPHTHALMIC
  • Status: approved

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FDA

  • Status: approved

Prednisolone 1% in other countries

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

Frequently asked questions

Is Prednisolone 1% approved in United States?

Yes. FDA authorised it on 30 May 1973; FDA has authorised it.

Who is the marketing authorisation holder for Prednisolone 1% in United States?

ABBVIE holds the US marketing authorisation.