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Generic competition · all medicines · read 12 November 2026

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

Minocycline Hydrochloride appears in 8 dosage-form groups in the FDA Orange Book as of 12 November 2026, with 12 generic makers listed as marketed across them. 4 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 0.2 and 20.7 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.
Minocycline Hydrochloride8 dosage-form groups in the Orange Book
12generic makers listed
  1. Minocycline Hydrochloride appears in 8 dosage-form groups in the FDA Orange Book as of 12 November 2026, with 12 generic makers listed as marketed across them.
  2. 4 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 0.2 and 20.7 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.

Tablet, Extended Release, Oral

Four or more generic makers listed

Every brand product here is listed as discontinued. 4 generic makers with 23 generic products listed as marketed; the first generic approval is dated 3 February 2009.

20052010201520202025203004brand 2006Sandoz Inc, first approval 13 August 2009Lupin Ltd, first approval 30 November 2011Aurobindo Pharma Ltd, first approval 19 November 2012Alkem Laboratories Ltd, first approval 28 September 2016data date
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end
Generic maker (applicant)First approvalProducts
Sandoz Inc13 August 20093
Lupin Ltd30 November 20114
Aurobindo Pharma Ltd19 November 20128
Alkem Laboratories Ltd28 September 20168

Patents and exclusivities still listed

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

Capsule, Oral

Four or more generic makers listed

Brand listed as marketed: Minocin. 6 generic makers with 15 generic products listed as marketed; the first generic approval is dated 31 July 1990.

19901995200020052010201520202025203006brand 1990Watson Laboratories Inc, first approval 30 December 1991Watson Laboratories Inc An Indirect Wholly Owned Sub Of Teva Pharmaceuticals Usa Inc, first approval 30 December 1991Zydus Worldwide Dmcc, first approval 2 March 1992Impax Laboratories Inc, first approval 23 March 1999Torrent Pharmaceuticals Ltd, first approval 30 November 2000Aurobindo Pharma Ltd, first approval 11 March 2008data date
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end
Generic maker (applicant)First approvalProducts
Watson Laboratories Inc30 December 19912
Watson Laboratories Inc An Indirect Wholly Owned Sub Of Teva Pharmaceuticals Usa Inc30 December 19911
Zydus Worldwide Dmcc2 March 19923
Impax Laboratories Inc23 March 19993
Torrent Pharmaceuticals Ltd30 November 20003
Aurobindo Pharma Ltd11 March 20083

Patents and exclusivities still listed

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

Tablet, Oral

Four or more generic makers listed

Every brand product here is listed as discontinued. 5 generic makers with 15 generic products listed as marketed; the first generic approval is dated 16 April 2003.

1980198519901995200020052010201520202025203005brand 1982Strides Pharma International Ag, first approval 16 April 2003Torrent Pharmaceuticals Ltd, first approval 6 January 2004Chartwell Rx Sciences Llc, first approval 26 December 2007Aurobindo Pharma Ltd, first approval 1 May 2020Regcon Holdings Llc, first approval 27 May 2022data date
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end
Generic maker (applicant)First approvalProducts
Strides Pharma International Ag16 April 20033
Torrent Pharmaceuticals Ltd6 January 20043
Chartwell Rx Sciences Llc26 December 20073
Aurobindo Pharma Ltd1 May 20203
Regcon Holdings Llc27 May 20223

Patents and exclusivities still listed

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

Capsule, Extended Release, Oral

Brand listed, no generic listed as marketed

Brand listed as marketed: Emrosi. No generic is listed as marketed.

201020152020202520302035204001brand 2012data datePatent 11364212 listed to expire 7 January 2039Patent 11191740 listed to expire 7 January 2039Patent 10905664 listed to expire 7 January 2039Patent 12594252 listed to expire 7 January 2039Exclusivity NP to 1 November 2027
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end

Patents and exclusivities still listed

  • 1 November 2027Exclusivity NP Emrosi
  • 7 January 2039Patent 11364212
  • 7 January 2039Patent 11191740
  • 7 January 2039Patent 10905664
  • 7 January 2039Patent 12594252

Aerosol, Foam, Topical

Brand listed, no generic listed as marketed

Brand listed as marketed: Amzeeq and Zilxi. No generic is listed as marketed.

20152020202520302035204001brand 2019data datePatent 10137200 listed to expire 1 October 2030Patent 8865139 listed to expire 1 October 2030Patent 9675700 listed to expire 1 October 2030Patent 8992896 listed to expire 1 October 2030Patent 10086080 listed to expire 1 October 2030Patent 10213512 listed to expire 1 October 2030Patent 10517882 listed to expire 1 October 2030Patent 10821187 listed to expire 1 October 2030Patent 8945516 listed to expire 1 October 2030Patent 10265404 listed to expire 1 October 2030Patent 10322186 listed to expire 1 October 2030Patent 10946101 listed to expire 1 October 2030Patent 12138311 listed to expire 1 October 2030Patent 12661407 listed to expire 1 October 2030Patent 10398641 listed to expire 8 September 2037Patent 10849847 listed to expire 8 September 2037
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end

Patents and exclusivities still listed

  • 1 October 2030Patent 10137200
  • 1 October 2030Patent 8865139 drug product
  • 1 October 2030Patent 9675700 drug product
  • 1 October 2030Patent 8992896 drug product
  • 1 October 2030Patent 10086080
  • 1 October 2030Patent 10213512 drug product
  • 1 October 2030Patent 10517882
  • 1 October 2030Patent 10821187

8 more patents are listed.

Injectable, Injection

Brand listed, no generic listed as marketed

Brand listed as marketed: Minocin. No generic is listed as marketed (1 generic product listed as discontinued).

202020252030203501data datePatent 9084802 listed to expire 12 May 2031Patent 9278105 listed to expire 12 May 2031Patent 12161656 listed to expire 12 May 2031Patent 11944634 listed to expire 16 October 2032
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end

Patents and exclusivities still listed

  • 12 May 2031Patent 9084802
  • 12 May 2031Patent 9278105
  • 12 May 2031Patent 12161656 drug product
  • 16 October 2032Patent 11944634 drug product

Powder, Extended Release, Dental

Brand listed, no generic listed as marketed

Brand listed as marketed: Arestin. No generic is listed as marketed.

200020052010201520202025203001brand 2001data date
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end

Patents and exclusivities still listed

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

Suspension, Oral

Nothing listed as marketed

Every brand product here is listed as discontinued. No generic is listed as marketed.

Patents and exclusivities still listed

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

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.