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Generic competition · all medicines · read 12 November 2026

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

Clonidine Hydrochloride appears in 5 dosage-form groups in the FDA Orange Book as of 12 November 2026, with 20 generic makers listed as marketed across them. 2 groups have 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 between 4 and 13 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.
Clonidine Hydrochloride5 dosage-form groups in the Orange Book
20generic makers listed
  1. Clonidine Hydrochloride appears in 5 dosage-form groups in the FDA Orange Book as of 12 November 2026, with 20 generic makers listed as marketed across them.
  2. 2 groups have 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 between 4 and 13 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.

Tablet, Oral

Four or more generic makers listed

Every brand product here is listed as discontinued. 9 generic makers with 29 generic products listed as marketed; the first generic approval is dated 8 July 1986.

198519901995200020052010201520202025203009Actavis Elizabeth Llc, first approval 16 December 1986Tp Anda Holdings Llc, first approval 4 September 1987Chartwell Molecules Llc, first approval 5 April 1988Aurobindo Pharma Ltd, first approval 31 August 1988Prinston Pharmaceutical Inc, first approval 9 March 2007Unichem Laboratories Ltd, first approval 26 August 2009Impax Laboratories Inc, first approval 27 August 2009Alembic Pharmaceuticals Ltd, first approval 6 December 2011Yung Shin Pharmaceutical Industrial Co Ltd, first approval 13 June 2013data date
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end
Generic maker (applicant)First approvalProducts
Actavis Elizabeth Llc16 December 19863
Tp Anda Holdings Llc4 September 19874
Chartwell Molecules Llc5 April 19883
Aurobindo Pharma Ltd31 August 19883
Prinston Pharmaceutical Inc9 March 20073
Unichem Laboratories Ltd26 August 20093
Impax Laboratories Inc27 August 20093
Alembic Pharmaceuticals Ltd6 December 20114
Yung Shin Pharmaceutical Industrial Co Ltd13 June 20133

Patents and exclusivities still listed

No unexpired patent or exclusivity is listed against the marketed brand products in this group.

Tablet, Extended Release, Oral

Four or more generic makers listed

Every brand product here is listed as discontinued. 7 generic makers with 7 generic products listed as marketed; the first generic approval is dated 30 September 2013.

20052010201520202025203007brand 2009Actavis Elizabeth Llc An Indirect Wholly Owned Sub Of Teva Pharmaceuticals Usa Inc, first approval 15 May 2015Chartwell Rx Sciences Llc, first approval 23 October 2017Ajanta Pharma Ltd, first approval 20 November 2017Xiamen Lp Pharmacuetical Co Ltd, first approval 20 November 2017Jubilant Generics Ltd, first approval 29 January 2018Somerset Therapeutics Llc, first approval 12 October 2018Novast Laboratories Ltd, first approval 5 March 2019data date
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end
Generic maker (applicant)First approvalProducts
Actavis Elizabeth Llc An Indirect Wholly Owned Sub Of Teva Pharmaceuticals Usa Inc15 May 20151
Chartwell Rx Sciences Llc23 October 20171
Ajanta Pharma Ltd20 November 20171
Xiamen Lp Pharmacuetical Co Ltd20 November 20171
Jubilant Generics Ltd29 January 20181
Somerset Therapeutics Llc12 October 20181
Novast Laboratories Ltd5 March 20191

Patents and exclusivities still listed

No unexpired patent or exclusivity is listed against the marketed brand products in this group.

Injectable, Injection

Four or more generic makers listed

Brand listed as marketed: Duraclon. 4 generic makers with 8 generic products listed as marketed; the first generic approval is dated 8 October 2009.

1995200020052010201520202025203004brand 1996Hikma Farmaceutica (Portugal) Sa, first approval 26 January 2011Fresenius Kabi Usa Llc, first approval 8 July 2011Xgen Pharmaceuticals Djb Inc, first approval 29 October 2013Zydus Pharmaceuticals Usa Inc, first approval 20 February 2014data date
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end
Generic maker (applicant)First approvalProducts
Hikma Farmaceutica (Portugal) Sa26 January 20112
Fresenius Kabi Usa Llc8 July 20112
Xgen Pharmaceuticals Djb Inc29 October 20132
Zydus Pharmaceuticals Usa Inc20 February 20142

Patents and exclusivities still listed

No unexpired patent or exclusivity is listed against the marketed brand products in this group.

Solution, Oral

Brand listed, no generic listed as marketed

Brand listed as marketed: Javadin and Qlonilik. No generic is listed as marketed.

20202025203020352040204501brand 2025data datePatent 12233049 listed to expire 15 July 2042Patent 12721837 listed to expire 15 July 2042Patent 12440474 listed to expire 15 July 2042Patent 12551466 listed to expire 22 August 2045
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end

Patents and exclusivities still listed

  • 15 July 2042Patent 12233049 drug product
  • 15 July 2042Patent 12721837 drug product
  • 15 July 2042Patent 12440474 drug product
  • 22 August 2045Patent 12551466 drug product

Suspension, Extended Release, Oral

Brand listed, no generic listed as marketed

Brand listed as marketed: Onyda Xr. No generic is listed as marketed.

20202025203020352040204501brand 2024data datePatent 8062667 listed to expire 29 March 2029Patent 11918689 listed to expire 28 July 2041Patent 12576032 listed to expire 28 July 2041
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end

Patents and exclusivities still listed

  • 29 March 2029Patent 8062667 drug product
  • 28 July 2041Patent 11918689 drug product
  • 28 July 2041Patent 12576032

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.