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Product profile · United States

EMBEDA

Patent Legal Status & Termination ↓  ·  Patent Litigation & Settlement History ↓

IngredientMORPHINE SULFATE; NALTREXONE HYDROCHLORIDE
Application typeNDA
Application022321
Product006
Dosage formCAPSULE, EXTENDED RELEASE
RouteORAL
Strength100MG;4MG
Approval date2009-08-13
Marketing statusDISCONTINUED
Status event—
Applicant—
Product source

Current GenericRadar decision

Year2012
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeEXCLUSIVITY
Anchor date2012-08-13
Patent anchor—
Exclusivity anchor2012-08-13
Protection date—
First Final ANDA—
Status event—

EMBEDA: NC full combination exclusivity ends 2012-08-13; S-016 abuse-deterrent label-change tail ends 2017-10-17, not full-product anchor. Later non-DS DP/U patents remain. 2012 DEEP_REVIEW.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
US86854432025-07-03U U-1508NNFORMULATION_OR_USE
TRUE_DS=N; DS-equivalent=N provisional. Legal expiry and termination are separate.
———
US86854442025-07-03DP —NNFORMULATION_OR_USE
TRUE_DS=N; DS-equivalent=N provisional. Legal expiry and termination are separate.
———
US76826332027-06-19U U-1510NNFORMULATION_OR_USE
TRUE_DS=N; DS-equivalent=N provisional. Legal expiry and termination are separate.
———
US76826342027-06-19DP —NNFORMULATION_OR_USE
TRUE_DS=N; DS-equivalent=N provisional. Legal expiry and termination are separate.
———
US81581562027-06-19U U-1510NNFORMULATION_OR_USE
TRUE_DS=N; DS-equivalent=N provisional. Legal expiry and termination are separate.
———
US88461042027-06-19DP —NNFORMULATION_OR_USE
TRUE_DS=N; DS-equivalent=N provisional. Legal expiry and termination are separate.
———
US88772472027-06-19DP —NNFORMULATION_OR_USE
TRUE_DS=N; DS-equivalent=N provisional. Legal expiry and termination are separate.
———
78159342027-12-12DP —NNFORMULATION_OR_USE
TRUE_DS=N; DS-equivalent=N provisional. Legal expiry and termination are separate.
———
US86234182029-11-07U U-1640NNFORMULATION_OR_USE
TRUE_DS=N; DS-equivalent=N provisional. Legal expiry and termination are separate.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
NC2009-08-132012-08-13Original new fixed-combination 3-year exclusivity: morphine sulfate/naltrexone hydrochlorideYY——Source
S-0162014-10-172017-10-17Supplement S-016: abuse-deterrent labeling/change-specific 3-year exclusivity. FDA states protection is tied to the combination of active moieties, but does not establish that all original approved uses are blocked.NN——Source

2026-10-24 · HISTORICAL_RECORDS_RECOVERED · Historical coverage: PARTIAL_HISTORY_RECOVERED

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.
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.