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Last Updated: April 18, 2024

FORTEO Drug Patent Profile


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When do Forteo patents expire, and when can generic versions of Forteo launch?

Forteo is a drug marketed by Lilly and is included in one NDA. There is one patent protecting this drug and one Paragraph IV challenge.

This drug has thirty-seven patent family members in twenty-five countries.

The generic ingredient in FORTEO is teriparatide. There are four drug master file entries for this compound. Five suppliers are listed for this compound. Additional details are available on the teriparatide profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Forteo

A generic version of FORTEO was approved as teriparatide by APOTEX on November 16th, 2023.

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Drug patent expirations by year for FORTEO
Drug Prices for FORTEO

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Recent Clinical Trials for FORTEO

Identify potential brand extensions & 505(b)(2) entrants

SponsorPhase
RANI TherapeuticsPhase 1
Radius Health, Inc.Phase 4
Daniel HorwitzPhase 4

See all FORTEO clinical trials

Pharmacology for FORTEO
Paragraph IV (Patent) Challenges for FORTEO
Tradename Dosage Ingredient Strength NDA ANDAs Submitted Submissiondate
FORTEO Injection teriparatide 250 mcg/mL, 2.4 mL prefilled Pen 021318 1 2015-07-27

US Patents and Regulatory Information for FORTEO

FORTEO is protected by one US patents.

Patents protecting FORTEO

Medication dispensing apparatus with spring-driven locking feature enabled by administration of final dose
Patent Number: ⤷  Try a Trial
Patent Expiration: ⤷  Try a Trial

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Lilly FORTEO teriparatide SOLUTION;SUBCUTANEOUS 021318-002 Jun 25, 2008 AP RX Yes Yes ⤷  Try a Trial ⤷  Try a Trial Y ⤷  Try a Trial
Lilly FORTEO teriparatide SOLUTION;SUBCUTANEOUS 021318-001 Nov 26, 2002 DISCN No No ⤷  Try a Trial ⤷  Try a Trial Y ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Expired US Patents for FORTEO

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Lilly FORTEO teriparatide SOLUTION;SUBCUTANEOUS 021318-002 Jun 25, 2008 ⤷  Try a Trial ⤷  Try a Trial
Lilly FORTEO teriparatide SOLUTION;SUBCUTANEOUS 021318-002 Jun 25, 2008 ⤷  Try a Trial ⤷  Try a Trial
Lilly FORTEO teriparatide SOLUTION;SUBCUTANEOUS 021318-002 Jun 25, 2008 ⤷  Try a Trial ⤷  Try a Trial
Lilly FORTEO teriparatide SOLUTION;SUBCUTANEOUS 021318-002 Jun 25, 2008 ⤷  Try a Trial ⤷  Try a Trial
Lilly FORTEO teriparatide SOLUTION;SUBCUTANEOUS 021318-001 Nov 26, 2002 ⤷  Try a Trial ⤷  Try a Trial
Lilly FORTEO teriparatide SOLUTION;SUBCUTANEOUS 021318-001 Nov 26, 2002 ⤷  Try a Trial ⤷  Try a Trial
Lilly FORTEO teriparatide SOLUTION;SUBCUTANEOUS 021318-002 Jun 25, 2008 ⤷  Try a Trial ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration

EU/EMA Drug Approvals for FORTEO

Company Drugname Inn Product Number / Indication Status Generic Biosimilar Orphan Marketing Authorisation Marketing Refusal
STADA Arzneimittel AG Movymia teriparatide EMEA/H/C/004368
Movymia is indicated in adults.Treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture. In postmenopausal women, a significant reduction in the incidence of vertebral and non vertebral fractures but not hip fractures has been demonstrated.Treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture.
Authorised no yes no 2017-01-11
Eli Lilly Nederland B.V. Forsteo teriparatide EMEA/H/C/000425
Treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture. In postmenopausal women, a significant reduction in the incidence of vertebral and nonvertebral fractures but not hip fractures has been demonstrated.Treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture.
Authorised no no no 2003-06-10
Gedeon Richter Plc. Terrosa teriparatide EMEA/H/C/003916
Terrosa is indicated in adults.Treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture. In postmenopausal women, a significant reduction in the incidence of vertebral and non vertebral fractures but not hip fractures has been demonstrated.Treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture.
Authorised no yes no 2017-01-04
EuroGenerics Holdings B.V. Qutavina teriparatide EMEA/H/C/005388
Qutavina is indicated in adults.Treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture. In postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures have been demonstrated.Treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture.
Withdrawn no yes no 2020-08-27
Theramex Ireland Limited Livogiva teriparatide EMEA/H/C/005087
Livogiva is indicated in adults.Treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture. In postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures have been demonstrated.Treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture.
Authorised no yes no 2020-08-27
Accord Healthcare S.L.U. Sondelbay teriparatide EMEA/H/C/005827
Sondelbay is indicated in adults.Treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture. In postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures have been demonstrated.Treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture.
Authorised no yes no 2022-03-24
Sun Pharmaceutical Industries Europe B.V. Teriparatide Sun teriparatide EMEA/H/C/005793
Teriparatide SUN is indicated in adults.Treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture (see section 5.1). In postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures has been demonstrated.Treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture (see section 5.1).
Authorised no no no 2022-11-18
>Company >Drugname >Inn >Product Number / Indication >Status >Generic >Biosimilar >Orphan >Marketing Authorisation >Marketing Refusal

International Patents for FORTEO

See the table below for patents covering FORTEO around the world.

Country Patent Number Title Estimated Expiration
Eurasian Patent Organization 200601801 УСТРОЙСТВО ДЛЯ ДОЗИРОВАНИЯ ЛЕКАРСТВЕННЫХ ПРЕПАРАТОВ С ПРУЖИННЫМ БЛОКИРУЮЩИМ УСТРОЙСТВОМ, ПРИВОДИМЫМ В ДЕЙСТВИЕ ПРИ ВВЕДЕНИИ ПОСЛЕДНЕЙ ДОЗЫ ⤷  Try a Trial
China 1198644 ⤷  Try a Trial
European Patent Office 1732629 APPAREIL D'ADMINISTRATION DE MEDICAMENT COMPRENANT UNE CARACTERISTIQUE DE VERROUILLAGE AU MOYEN D'UN RESSORT POUR L'ADMINISTRATION D'UNE DOSE FINALE (MEDICATION DISPENSING APPARATUS WITH SPRING-DRIVEN LOCKING FEATURE ENABLED BY ADMINISTRATION OF FINAL DOSE) ⤷  Try a Trial
South Korea 20060131946 MEDICATION DISPENSING APPARATUS WITH SPRING-DRIVEN LOCKING FEATURE ENABLED BY ADMINISTRATION OF FINAL DOSE ⤷  Try a Trial
Lithuania 1732629 ⤷  Try a Trial
South Korea 20010072763 ⤷  Try a Trial
Turkey 200003455 ⤷  Try a Trial
>Country >Patent Number >Title >Estimated Expiration

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