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Generic competition · all medicines · read 12 November 2026

Is there a generic of Losartan Potassium, and who makes it?

Losartan Potassium appears in 2 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 15 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.
Losartan Potassium2 dosage-form groups in the Orange Book
16generic makers listed
  1. Losartan Potassium appears in 2 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 15 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

Brand listed as marketed: Cozaar. 16 generic makers with 48 generic products listed as marketed; the first generic approval is dated 6 April 2010.

19952000200520102015202020252030016brand 1995Aiping Pharmaceutical Inc, first approval 6 October 2010Alembic Pharmaceuticals Ltd, first approval 6 October 2010Aurobindo Pharma Ltd, first approval 6 October 2010Chartwell Rx Sciences Llc, first approval 6 October 2010Lupin Ltd, first approval 6 October 2010Strides Pharma Global Pte Ltd, first approval 6 October 2010Watson Laboratories Inc, first approval 6 October 2010Zydus Pharmaceuticals Usa Inc, first approval 6 October 2010Prinston Pharmaceutical Inc, first approval 6 June 2011Macleods Pharmaceuticals Ltd, first approval 30 May 2012Jubilant Cadista Pharmaceuticals Inc, first approval 18 September 2012Hetero Labs Ltd Unit V, first approval 12 August 2015Unichem Laboratories Ltd, first approval 14 October 2015Granules India Ltd, first approval 23 February 2023Msn Laboratories Private Ltd, first approval 14 August 2023Graviti Pharmaceuticals Private Ltd, first approval 19 September 2025data date
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end
Generic maker (applicant)First approvalProducts
Aiping Pharmaceutical Inc6 October 20103
Alembic Pharmaceuticals Ltd6 October 20103
Aurobindo Pharma Ltd6 October 20103
Chartwell Rx Sciences Llc6 October 20103
Lupin Ltd6 October 20103
Strides Pharma Global Pte Ltd6 October 20103
Watson Laboratories Inc6 October 20103
Zydus Pharmaceuticals Usa Inc6 October 20103
Prinston Pharmaceutical Inc6 June 20113
Macleods Pharmaceuticals Ltd30 May 20123
Jubilant Cadista Pharmaceuticals Inc18 September 20123
Hetero Labs Ltd Unit V12 August 20153

4 more makers are listed in the data.

Patents and exclusivities still listed

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

Suspension, Oral

Brand listed, no generic listed as marketed

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

20202025203020352040204501brand 2025data datePatent 12156869 listed to expire 7 October 2041Patent 12605365 listed to expire 7 October 2041Patent 11890273 listed to expire 7 October 2041
generic makers listed as marketed, by first approvallisted patent expiryexclusivity end

Patents and exclusivities still listed

  • 7 October 2041Patent 12156869 drug product
  • 7 October 2041Patent 12605365 drug product
  • 7 October 2041Patent 11890273 drug product

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.