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Product profile · United States

MYFEMBREE

 ·  Patent Litigation & Settlement History ↓

IngredientESTRADIOL; NORETHINDRONE ACETATE; RELUGOLIX
Application typeNDA
Application214846
Product001
Dosage formTABLET
RouteORAL
Strength1MG;0.5MG;40MG
Approval date2021-05-26
Marketing statusPrescription
Status event—
ApplicantSUMITOMO PHARMA AM
Product source

Current GenericRadar decision

Year2029
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeTRUE_DS_PATENT
Anchor date2029-01-28
Patent anchor2029-01-28
Exclusivity anchor2025-12-18
Protection date2042-11-05
First Final ANDA—
Status event—

POST_ANCHOR_RIGHTS_EXIST; US:NDA:214846:001; exact Final ANDA not verified; not proof of generic absence

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
80582802026-01-28DS/DP —YNTRUE_DS
| B1C03P8 issued-claim review2026-10-15: TRUE_DS
———
80582802026-01-28ORANGE_BOOK —YNTRUE_DS
English description not available.
———
73009352029-01-28DS —YNTRUE_DS
| B1C03P8 issued-claim review2026-10-15: TRUE_DS
———
73009352029-01-28ORANGE_BOOK —YNTRUE_DS
English description not available.
———
117951782033-09-27DS/DP —NNDP
| B1C03P8 issued-claim review2026-10-15: DP
———
117951782033-09-27ORANGE_BOOK —NNDP
English description not available.
———
123257142033-09-27DS/DP —NNDP
| B1C03P8 issued-claim review2026-10-15: DP
———
123257142033-09-27ORANGE_BOOK —NNDP
English description not available.
———
110335512037-09-29U U-3129NNU
| B1C03P8 issued-claim review2026-10-15: U
———
110335512037-09-29ORANGE_BOOK U-3129NNU
English description not available.
———
119576842037-09-29U U-3129NNU
| B1C03P8 issued-claim review2026-10-15: U
———
119576842037-09-29ORANGE_BOOK U-3129NNU
English description not available.
———
117938122038-05-03U U-2360NNU
| B1C03P8 issued-claim review2026-10-15: U
———
117938122038-05-03ORANGE_BOOK U-2360NNU
English description not available.
———
125514472042-11-05DP —NNDP
| B1C03P8 issued-claim review2026-10-15: DP
———
125514472042-11-05ORANGE_BOOK —NNDP
English description not available.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
NP2021-05-262024-05-26English description not available.YY2024-05-26
NCE
Full coverage date: 2024-05-26
Source
I-8982022-08-052025-08-05English description not available.NN—
NCE
Full coverage date: —
Source
NCE2020-12-182025-12-18English description not available.YY2025-12-18
NCE
Full coverage date: 2025-12-18
Source
M-2892023-01-272026-01-27English description not available.NN——Source
M-2892023-01-272026-01-27English description not available.NN—
NCE
Full coverage date: —
Source

2026-10-10 · CURRENT_SOURCE_RECORDS_FOUND · Historical coverage: NOT_COMPLETE

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
No generic approval facts are linked to this product.

Market Entry Information

API filings, authorized generics and linked regulatory milestones.

API Master Files & Certifications 0 records

Ingredient-level registrations from linked public manufacturer portfolios. A filing does not establish supply to this finished product. DMFs are not FDA approvals.

APIHolder / manufacturerHolder countryFiling typeNumberStatusFiled dateAvailable for referenceSourceLast verified
No master-file or certification records are linked through public manufacturer portfolios.

Authorized Generics 0 records

Authorized generics are shown separately from independent ANDA approvals.

Application / productApplicantEvent / status First marketed Product mappingSourceLast verified
No authorized-generic records are linked to this product.

Tentative ANDA Approvals 0 records

Tentative approval is not final approval. Historical tentative approvals remain visible after a linked final approval.

Application / productApplicantEvent / status Tentative date Follow-up final approvalProduct mappingSourceLast verified
No tentative-approval records are linked to this product.

Paragraph IV Challenges 0 records

Paragraph IV challenges below are sourced from legal records separately from FDA approvals. An ANDA filing, lawsuit or settlement does not establish final approval or commercial launch.

Application / productApplicantEvent / status Certification event date Product mappingSourceLast verified
No structured Paragraph IV certification events are linked in the available approval evidence.

Final ANDA Approvals 0 records

Approval dates do not establish commercial launch. Product mapping is shown for each linked record.

Application / productApplicantEvent / status Final approval date Product mappingSourceLast verified
No final-approval records are linked to this product.
Decision evidence (13)
TypeDateRoleBasisSource
PATENT2026-01-28HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2029-01-28CANONICAL_ANCHOREnglish description not available.Source
PATENT2033-09-27FTO_TAILEnglish description not available.Source
PATENT2033-09-27FTO_TAILEnglish description not available.Source
PATENT2037-09-29FTO_TAILEnglish description not available.Source
PATENT2037-09-29FTO_TAILEnglish description not available.Source
PATENT2038-05-03FTO_TAILEnglish description not available.Source
PATENT2042-11-05FTO_TAILEnglish description not available.Source
REGULATORY_EXCLUSIVITY—REGULATORY_SCOPE_CONTEXTEnglish description not available.Source
REGULATORY_EXCLUSIVITY—REGULATORY_SCOPE_CONTEXTEnglish description not available.Source
REGULATORY_EXCLUSIVITY—REGULATORY_SCOPE_CONTEXTEnglish description not available.Source
REGULATORY_EXCLUSIVITY—REGULATORY_SCOPE_CONTEXTEnglish description not available.Source
REGULATORY_STATUS2029-01-28CANONICAL_DECISIONPOST_ANCHOR_RIGHTS_EXIST; US:NDA:214846:001; exact Final ANDA not verified; not proof of generic absenceSource
Independent legal-event information

Litigation & Settlement History

Settlement launch rights generally apply only to the named parties and product scope. These records do not change GenericRadar patent/exclusivity anchors or current decisions.

No litigation or settlement record currently linked to this product.