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Generic competition · all medicines · read 12 November 2026

Is there a generic of Oxymetazoline Hydrochloride, and who makes it?

Oxymetazoline Hydrochloride appears in 2 dosage-form groups in the FDA Orange Book as of 12 November 2026, with 1 generic maker listed as marketed across them. 1 group has a brand listed as marketed and no generic listed as marketed. The data does not state why, and it does not state that one is coming. Where both are dated, the first generic approval came 4.7 years after the first brand approval. This is the Orange Book's listing, not a forecast.

Compiled and checked by Vincent Wesley Couey (ORCID 0009-0005-6869-308X) from the Orange Book data files, downloaded 12 November 2026.

Not medical advice. This page reports what the FDA's Orange Book lists, not what a pharmacy has in stock, what anything costs, or whether a generic is right for you. Ask your pharmacist or prescriber about your own medicine.
Oxymetazoline Hydrochloride2 dosage-form groups in the Orange Book
1generic maker listed
  1. Oxymetazoline Hydrochloride appears in 2 dosage-form groups in the FDA Orange Book as of 12 November 2026, with 1 generic maker listed as marketed across them.
  2. 1 group has a brand listed as marketed and no generic listed as marketed. The data does not state why, and it does not state that one is coming.
  3. Where both are dated, the first generic approval came 4.7 years after the first brand approval.
  4. Patents and exclusivities are shown as listed by the application holder; the Orange Book does not rule on them, and a listed patent is not a statement that a generic is blocked. This says nothing about price, supply or quality.

Solution/Drops, Ophthalmic

Brand listed, no generic listed as marketed

Brand listed as marketed: Upneeq and Visine L.r.. No generic is listed as marketed.

19851990199520002005201020152020202520302035204001brand 1986data datePatent 8357714 listed to expire 26 August 2031Patent 9867808 listed to expire 26 August 2031Patent 10912765 listed to expire 26 August 2031Patent 11324722 listed to expire 16 December 2039Patent 10940138 listed to expire 16 December 2039Patent 10799481 listed to expire 16 December 2039Patent 11701343 listed to expire 16 December 2039Patent 12648930 listed to expire 16 December 2039Patent 10898573 listed to expire 16 December 2039Patent 12605363 listed to expire 16 December 2039Patent 10814001 listed to expire 16 December 2039Patent 11311515 listed to expire 16 December 2039Patent 11541036 listed to expire 16 December 2039Patent 11103482 listed to expire 16 December 2039
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end

Patents and exclusivities still listed

  • 26 August 2031Patent 8357714
  • 26 August 2031Patent 9867808
  • 26 August 2031Patent 10912765
  • 16 December 2039Patent 11324722
  • 16 December 2039Patent 10940138
  • 16 December 2039Patent 10799481
  • 16 December 2039Patent 11701343
  • 16 December 2039Patent 12648930

6 more patents are listed.

Cream, Topical

One to three generic makers listed

Brand listed as marketed: Rhofade. 1 generic maker with 1 generic product listed as marketed; the first generic approval is dated 4 October 2021.

2015202020252030203501brand 2017Sun Pharma Canada Inc, first approval 4 October 2021data datePatent 7812049 listed to expire 2 May 2028Patent 8883838 listed to expire 1 December 2031Patent 9974773 listed to expire 11 June 2035Patent 10751325 listed to expire 11 June 2035Patent 12350255 listed to expire 11 June 2035Patent 10335391 listed to expire 11 June 2035Patent 11517560 listed to expire 11 June 2035
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end
Generic maker (applicant)First approvalProducts
Sun Pharma Canada Inc4 October 20211

Patents and exclusivities still listed

  • 2 May 2028Patent 7812049
  • 1 December 2031Patent 8883838 drug product
  • 11 June 2035Patent 9974773
  • 11 June 2035Patent 10751325
  • 11 June 2035Patent 12350255
  • 11 June 2035Patent 10335391
  • 11 June 2035Patent 11517560

US Food and Drug Administration, Orange Book data files, downloaded 12 November 2026. A listed patent is not a ruling that a generic is blocked, and no figure here says anything about price, supply or quality. Check the Orange Book.

Where can you go from this result?

Open it in the check to search another medicine, or see every brand with no generic listed. The FDA explains generic approval in how generic drugs are approved and the FDA generic drug facts, and the Orange Book itself is the FDA Orange Book. To check what is available now, ask your pharmacist, and see the FDA drug shortages page.