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Product profile · United States

POMALYST

 ·  Patent Litigation & Settlement History ↓

IngredientPOMALIDOMIDE
Application typeNDA
Application204026
Product001
Dosage formCAPSULE
RouteORAL
Strength1MG
Approval date2013-02-08
Marketing statusPrescription
Status event—
ApplicantBRISTOL
Product source

Current GenericRadar decision

Year2020
SelectionEXISTING_GENERIC
ReviewDISQUALIFIED
Anchor typeFINAL_ANDA
Anchor date2020-10-30
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2020-10-30
Status event—

Exact product/strength Final ANDA confirmed. Date is earliest verified official product approval for the batch. AG and tentative excluded. Approval date is not commercial launch date. No DS classification asserted.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
105559392030-05-19DP ————
———
99934672030-05-19DP ————
———
105559392030-11-19— ————
—2030-11-19—
99934672030-11-19— ————
—2030-11-19—
88284272031-06-21DS/DP ————
———
88284272031-12-21— ————
—2031-12-21—

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
ODE-296—2027-05-14————Source
ODE-297—2027-05-14————Source
PED—2027-11-14————Source

2026-10-10 · CURRENT_SOURCE_RECORDS_FOUND · Historical coverage: NOT_COMPLETE

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
210111 / 001FINAL_APPROVAL · FINAL_APPROVED2020-10-30—BRECKENRIDGE PHARMACEUTICAL INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
210249 / 001FINAL_APPROVAL · FINAL_APPROVED2020-10-30—EUGIA PHARMA SPECIALITIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
210275 / 001FINAL_APPROVAL · FINAL_APPROVED2022-01-26—MYLAN PHARMACEUTICALS INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
209956 / 001FINAL_APPROVAL · FINAL_APPROVED2022-05-04—TEVA PHARMACEUTICALS USA INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
210164 / 001FINAL_APPROVAL · FINAL_APPROVED2024-06-11—APOTEX INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
210236 / 001FINAL_APPROVAL · FINAL_APPROVED2024-09-26—HETERO LABS LTD UNIT VNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
210232 / 001FINAL_APPROVAL · FINAL_APPROVED2026-08-31—SUN PHARMA INDUSTRIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
213234 / 001FINAL_APPROVAL · FINAL_APPROVED2026-08-31—DR REDDYS LABORATORIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
219718 / 001FINAL_APPROVAL · FINAL_APPROVED2026-08-31—CIPLA LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
220741 / 001FINAL_APPROVAL · FINAL_APPROVED2026-08-31—SANDOZ INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource

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 10 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
210111 / 001BRECKENRIDGE PHARMACEUTICAL INCFINAL_APPROVAL · FINAL_APPROVED2020-10-30 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
210249 / 001EUGIA PHARMA SPECIALITIES LTDFINAL_APPROVAL · FINAL_APPROVED2020-10-30 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
210275 / 001MYLAN PHARMACEUTICALS INCFINAL_APPROVAL · FINAL_APPROVED2022-01-26 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
209956 / 001TEVA PHARMACEUTICALS USA INCFINAL_APPROVAL · FINAL_APPROVED2022-05-04 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
210164 / 001APOTEX INCFINAL_APPROVAL · FINAL_APPROVED2024-06-11 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
210236 / 001HETERO LABS LTD UNIT VFINAL_APPROVAL · FINAL_APPROVED2024-09-26 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
210232 / 001SUN PHARMA INDUSTRIES LTDFINAL_APPROVAL · FINAL_APPROVED2026-08-31 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
213234 / 001DR REDDYS LABORATORIES LTDFINAL_APPROVAL · FINAL_APPROVED2026-08-31 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
219718 / 001CIPLA LTDFINAL_APPROVAL · FINAL_APPROVED2026-08-31 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
220741 / 001SANDOZ INCFINAL_APPROVAL · FINAL_APPROVED2026-08-31 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (1)
TypeDateRoleBasisSource
GENERIC2020-10-30TERMINAL_GENERIC_BASISExact product/strength Final ANDA confirmed. Date is earliest verified official product approval for the batch. AG and tentative excluded. Approval date is not commercial launch date. No DS classification asserted.Source
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.