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Generic competition · all medicines · read 12 November 2026

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

Amantadine Hydrochloride appears in 5 dosage-form groups in the FDA Orange Book as of 12 November 2026, with 16 generic makers 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 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.
Amantadine Hydrochloride5 dosage-form groups in the Orange Book
16generic makers listed
  1. Amantadine Hydrochloride appears in 5 dosage-form groups in the FDA Orange Book as of 12 November 2026, with 16 generic makers 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 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.

Capsule, Oral

Four or more generic makers listed

Every brand product here is listed as discontinued. 11 generic makers with 11 generic products listed as marketed; the first generic approval is dated 5 August 1986.

1985199019952000200520102015202020252030011Upsher Smith Laboratories Llc, first approval 5 August 1986Sandoz Inc, first approval 18 February 1987Bionpharma Inc, first approval 29 May 2008Zydus Pharmaceuticals Usa Inc, first approval 31 May 2016Strides Pharma Global Pte Ltd, first approval 7 June 2017Heritage Pharma Labs Inc, first approval 12 June 2017Alembic Pharmaceuticals Ltd, first approval 21 June 2017Rising Pharma Holdings Inc, first approval 2 March 2020Rubicon Research Ltd, first approval 21 May 2020Onesource Softgels Pte Ltd, first approval 18 February 2022Humanwell Puracap Pharmaceutical Wuhan Co Ltd, first approval 20 December 2022data date
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end
Generic maker (applicant)First approvalProducts
Upsher Smith Laboratories Llc5 August 19861
Sandoz Inc18 February 19871
Bionpharma Inc29 May 20081
Zydus Pharmaceuticals Usa Inc31 May 20161
Strides Pharma Global Pte Ltd7 June 20171
Heritage Pharma Labs Inc12 June 20171
Alembic Pharmaceuticals Ltd21 June 20171
Rising Pharma Holdings Inc2 March 20201
Rubicon Research Ltd21 May 20201
Onesource Softgels Pte Ltd18 February 20221
Humanwell Puracap Pharmaceutical Wuhan Co Ltd20 December 20221

Patents and exclusivities still listed

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

Syrup, Oral

Four or more generic makers listed

Every brand product here is listed as discontinued. 4 generic makers with 5 generic products listed as marketed; the first generic approval is dated 30 October 1990.

19901995200020052010201520202025203004Chartwell Rx Sciences Llc, first approval 28 June 1993Aurobindo Pharma Usa Inc, first approval 28 October 1994Pharmaceutical Associates Inc, first approval 17 July 1995Pharmobedient Consulting Llc, first approval 24 December 1998data date
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end
Generic maker (applicant)First approvalProducts
Chartwell Rx Sciences Llc28 June 19931
Aurobindo Pharma Usa Inc28 October 19941
Pharmaceutical Associates Inc17 July 19951
Pharmobedient Consulting Llc24 December 19982

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 5 generic products listed as marketed; the first generic approval is dated 16 December 2002.

200020052010201520202025203005Upsher Smith Laboratories Llc, first approval 16 December 2002Strides Pharma Global Pte Ltd, first approval 9 June 2017Pharmobedient Consulting Llc, first approval 10 March 2020Alembic Pharmaceuticals Ltd, first approval 15 October 2020Zhejiang Jutai Pharmaceutical Co Ltd, first approval 26 September 2024data date
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end
Generic maker (applicant)First approvalProducts
Upsher Smith Laboratories Llc16 December 20021
Strides Pharma Global Pte Ltd9 June 20171
Pharmobedient Consulting Llc10 March 20201
Alembic Pharmaceuticals Ltd15 October 20201
Zhejiang Jutai Pharmaceutical Co Ltd26 September 20241

Patents and exclusivities still listed

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

Tablet, Extended Release, Oral

Nothing listed as marketed

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

201520202025203001brand 2018data 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.

Capsule, Extended Release, Oral

Brand listed, no generic listed as marketed

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

20152020202520302035204001brand 2017data datePatent 8389578 listed to expire 22 January 2028Patent 9867792 listed to expire 2 December 2030Patent 9867791 listed to expire 2 December 2030Patent 9877933 listed to expire 2 December 2030Patent 8741343 listed to expire 2 December 2030Patent 9867793 listed to expire 2 December 2030Patent 11197835 listed to expire 2 December 2030Patent 10646456 listed to expire 17 June 2034Patent 11903908 listed to expire 17 June 2034Patent 10154971 listed to expire 4 December 2034Patent 12233033 listed to expire 23 August 2038Patent 11077073 listed to expire 23 August 2038Patent 11065213 listed to expire 23 August 2038
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end

Patents and exclusivities still listed

  • 22 January 2028Patent 8389578
  • 2 December 2030Patent 9867792
  • 2 December 2030Patent 9867791
  • 2 December 2030Patent 9877933
  • 2 December 2030Patent 8741343
  • 2 December 2030Patent 9867793
  • 2 December 2030Patent 11197835
  • 17 June 2034Patent 10646456

5 more patents are listed.

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.