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Product profile · United States

ZEPBOUND

 ·  Patent Litigation & Settlement History ↓

IngredientTIRZEPATIDE
Application typeNDA
Application217806
Product010
Dosage formSOLUTION
RouteSUBCUTANEOUS
Strength10MG/0.5ML (10MG/0.5ML)
Approval date2024-03-28
Marketing statusPrescription
Status event—
ApplicantELI LILLY AND CO
Product source

Current GenericRadar decision

Year2036
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeTRUE_DS_PATENT
Anchor date2036-05-13
Patent anchor2036-05-13
Exclusivity anchor2027-05-13
Protection date2039-07-22
First Final ANDA—
Status event—

POST_ANCHOR_RIGHTS_EXIST; US:NDA:217806:010; exact Final ANDA not verified; not proof of generic absence

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
94747802036-05-13DS/DP —YNTRUE_DS
| B1C03P8 issued-claim review2026-10-15: TRUE_DS
———
94747802036-05-13ORANGE_BOOK —YNTRUE_DS
English description not available.
———
113578202039-06-14DP —NNDP
| B1C03P8 issued-claim review2026-10-15: DP
———
113578202039-06-14ORANGE_BOOK —NNDP
English description not available.
———
119186232039-06-14U U-3855NNU
| B1C03P8 issued-claim review2026-10-15: U
———
119186232039-06-14ORANGE_BOOK U-3855NNU
English description not available.
———
124537562039-06-14DP —NNDP
| B1C03P8 issued-claim review2026-10-15: DP
———
124537562039-06-14ORANGE_BOOK —NNDP
English description not available.
———
126294042039-06-14DP/U U-4532NNDP
| B1C03P8 issued-claim review2026-10-15: DP
———
126294042039-06-14DP/U U-4531NNDP
| B1C03P8 issued-claim review2026-10-15: DP
———
126294042039-06-14ORANGE_BOOK U-4531;U-4532NNDP
English description not available.
———
123433822039-07-22U U-4227NNU
| B1C03P8 issued-claim review2026-10-15: U
———
123433822039-07-22U U-4409NNU
| B1C03P8 issued-claim review2026-10-15: U
———
123433822039-07-22U U-4410NNU
| B1C03P8 issued-claim review2026-10-15: U
———
123433822039-07-22U U-4228NNU
| B1C03P8 issued-claim review2026-10-15: U
———
123433822039-07-22ORANGE_BOOK U-4227;U-4228;U-4409;U-4410NNU
English description not available.
———
124537582039-07-22U U-4309NNU
| B1C03P8 issued-claim review2026-10-15: U
———
124537582039-07-22U U-4308NNU
| B1C03P8 issued-claim review2026-10-15: U
———
124537582039-07-22U U-4310NNU
| B1C03P8 issued-claim review2026-10-15: U
———
124537582039-07-22U U-4311NNU
| B1C03P8 issued-claim review2026-10-15: U
———
124537582039-07-22ORANGE_BOOK U-4308;U-4309;U-4310;U-4311NNU
English description not available.
———
126167402039-07-22U U-4499NNU
| B1C03P8 issued-claim review2026-10-15: U
———
126167402039-07-22U U-4497NNU
| B1C03P8 issued-claim review2026-10-15: U
———
126167402039-07-22U U-4498NNU
| B1C03P8 issued-claim review2026-10-15: U
———
126167402039-07-22ORANGE_BOOK U-4497;U-4498;U-4499NNU
English description not available.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
NCE2022-05-132027-05-13English description not available.YY2027-05-13—Source
NCE2022-05-132027-05-13English description not available.YY2027-05-13
NCE
Full coverage date: 2027-05-13
Source
M-822024-10-182027-10-18English description not available.NN——Source
M-822024-10-182027-10-18English description not available.NN—
NCE
Full coverage date: —
Source
I-9582024-12-202027-12-20English description not available.NN——Source
I-9582024-12-202027-12-20English 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 (12)
TypeDateRoleBasisSource
PATENT2036-05-13CANONICAL_ANCHOREnglish description not available.Source
PATENT2039-06-14FTO_TAILEnglish description not available.Source
PATENT2039-06-14FTO_TAILEnglish description not available.Source
PATENT2039-06-14FTO_TAILEnglish description not available.Source
PATENT2039-06-14FTO_TAILEnglish description not available.Source
PATENT2039-07-22FTO_TAILEnglish description not available.Source
PATENT2039-07-22FTO_TAILEnglish description not available.Source
PATENT2039-07-22FTO_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_STATUS2036-05-13CANONICAL_DECISIONPOST_ANCHOR_RIGHTS_EXIST; US:NDA:217806:010; 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.