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Product profile · United States

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 ·  Patent Litigation & Settlement History ↓

IngredientLEVONORGESTREL
Application typeNDA
Application206229
Product001
Dosage formSYSTEM
RouteINTRAUTERINE
Strength52MG
Approval date2015-02-26
Marketing statusPrescription
Status event—
ApplicantMEDICINES360
Product source

Current GenericRadar decision

Year2018
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeREGULATORY_EXCLUSIVITY
Anchor date2018-02-26
Patent anchor—
Exclusivity anchor2018-02-26
Protection date2040-09-07
First Final ANDA—
Status event—

POST_ANCHOR_RIGHTS_REMAIN; canonical=2018-02-26; exact Final ANDA not directly identified; not generic absence

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
120049922033-10-06DS —NNDP
| B1C0201 issued-claim review2026-10-14: DP
———
120049922033-10-06ORANGE_BOOK —NNDP
English description not available.
———
110901862033-10-24U U-2348NNU
| B1C0201 issued-claim review2026-10-14: U
———
110901862033-10-24ORANGE_BOOK U-2348NNU
English description not available.
———
100288582034-03-22DP/U U-2348NNDP
| B1C0201 issued-claim review2026-10-14: DP
———
100288582034-03-22ORANGE_BOOK U-2348NNDP
English description not available.
———
115713282040-09-07DP —NNDP
| B1C0201 issued-claim review2026-10-14: DP
———
115713282040-09-07ORANGE_BOOK —NNDP
English description not available.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
NP2015-02-262018-02-26English description not available.YY2018-02-26Source
I-9172023-06-292026-06-29English description not available.NN——Source
I-9172023-06-292026-06-29English description not available.NN—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 (7)
TypeDateRoleBasisSource
PATENT2033-10-06FTO_TAILEnglish description not available.Source
PATENT2033-10-24FTO_TAILEnglish description not available.Source
PATENT2034-03-22FTO_TAILEnglish description not available.Source
PATENT2040-09-07FTO_TAILEnglish description not available.Source
REGULATORY_EXCLUSIVITY—FTO_TAILEnglish description not available.Source
REGULATORY_EXCLUSIVITY—CANONICAL_ANCHOREnglish description not available.Source
REGULATORY_STATUS2018-02-26CANONICAL_DECISIONPOST_ANCHOR_RIGHTS_REMAIN; canonical=2018-02-26; exact Final ANDA not directly identified; not 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.