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Product profile · United States

REZDIFFRA

 ·  Patent Litigation & Settlement History ↓

IngredientRESMETIROM
Application typeNDA
Application217785
Product003
Dosage formTABLET
RouteORAL
Strength100MG
Approval date2024-03-14
Marketing statusPrescription
Status event—
ApplicantMADRIGAL
Product source

Current GenericRadar decision

Year2033
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeDS_EQUIVALENT_PATENT
Anchor date2033-09-17
Patent anchor2033-09-17
Exclusivity anchor2029-03-14
Protection date2045-02-04
First Final ANDA—
Status event—

POST_ANCHOR_RIGHTS_EXIST; US:NDA:217785:003; exact Final ANDA not verified; not proof of generic absence

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
74528822027-09-12DS/DP —YNTRUE_DS
| B1C03P7 issued-claim review2026-10-15: TRUE_DS
———
74528822027-09-12ORANGE_BOOK —YNTRUE_DS
English description not available.
———
103765172033-09-17U U-3861NNDP
| B1C03P7 issued-claim review2026-10-15: DP
———
103765172033-09-17ORANGE_BOOK U-3861NNDP
English description not available.
———
115649262033-09-17DS/DP/U U-3861NNDP
| B1C03P7 issued-claim review2026-10-15: DP
———
115649262033-09-17ORANGE_BOOK U-3861NNDP
English description not available.
———
119864812033-09-17U U-3861NYU
| B1C03P7 issued-claim review2026-10-15: U
———
119864812033-09-17ORANGE_BOOK U-3861NYU
English description not available.
———
92668612033-09-17DS/DP —NNDP
| B1C03P7 issued-claim review2026-10-15: DP
———
92668612033-09-17ORANGE_BOOK —NNDP
English description not available.
———
126613592042-01-28U U-4568NNU
| B1C03P7 issued-claim review2026-10-15: U
———
126613592042-01-28ORANGE_BOOK U-4568NNU
English description not available.
———
123771042045-02-04U U-3861NNU
| B1C03P7 issued-claim review2026-10-15: U
———
123771042045-02-04ORANGE_BOOK U-3861NNU
English description not available.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
NCE2024-03-142029-03-14English description not available.YY2029-03-14—Source
NCE2024-03-142029-03-14English description not available.YY2029-03-14
NCE
Full coverage date: 2029-03-14
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 (9)
TypeDateRoleBasisSource
PATENT2027-09-12HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2033-09-17HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2033-09-17HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2033-09-17CANONICAL_ANCHOREnglish description not available.Source
PATENT2033-09-17HISTORICAL_CONTEXTEnglish description not available.Source
PATENT2042-01-28FTO_TAILEnglish description not available.Source
PATENT2045-02-04FTO_TAILEnglish description not available.Source
REGULATORY_EXCLUSIVITY—REGULATORY_SCOPE_CONTEXTEnglish description not available.Source
REGULATORY_STATUS2033-09-17CANONICAL_DECISIONPOST_ANCHOR_RIGHTS_EXIST; US:NDA:217785:003; 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.