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Product profile · United States

MYCAPSSA

 ·  Patent Litigation & Settlement History ↓

IngredientOCTREOTIDE ACETATE
Application typeNDA
Application208232
Product001
Dosage formCAPSULE, DELAYED RELEASE
RouteORAL
StrengthEQ 20MG BASE
Approval date2020-06-26
Marketing statusPrescription
Status event—
ApplicantCHIESI
Product source

Current GenericRadar decision

Year2036
SelectionDEEP_REVIEW
ReviewFINAL_CHECKING
Anchor typeDS_EQUIVALENT
Anchor date2036-02-03
Patent anchor2036-02-03
Exclusivity anchor2027-06-26
Protection date—
First Final ANDA—
Status event—

GNR judgment: DEEP_REVIEW. Reference year: 2036. Anchor type: DS_EQUIVALENT. Patent anchor: 2036-02-03. Exclusivity anchor: 2027-06-26. Anchor date: 2036-02-03. Patent tail: yes. Exclusivity tail: no. Review status: FINAL_CHECKING. Historical detailed rationale is retained in the evidence snapshot; this is a structured English summary, not a literal translation.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
119694712029-09-17DP ————
———
119865292029-09-17U U-2857———
———
83291982029-09-17DP ————
———
85356952029-09-17U U-2857———
———
92658122029-09-17DP ————
———
95662462029-09-17DP ————
———
102387092036-02-03U U-2857———
———
106953972036-02-03U U-2857———
———
110521262036-02-03U U-2857———
———
113380112036-02-03U U-2857———
———
115109632036-02-03U U-2857———
———
118575952036-02-03U U-3784———
———
122460542036-02-03U U-2857———
———
122514182036-02-03U U-2857———
———
111414572040-12-28U U-3232———
———
118903162040-12-28U U-3232———
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
ODE-474—2027-06-26————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.
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.