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Product profile · United States

SILENOR

 ·  Patent Litigation & Settlement History ↓

IngredientDOXEPIN HYDROCHLORIDE
Application typeNDA
Application022036
Product001
Dosage formTABLET
RouteORAL
StrengthEQ 3MG BASE
Approval date2010-03-17
Marketing statusPrescription
Status event—
ApplicantCURRAX
Product source

Current GenericRadar decision

Year2013
SelectionEXISTING_GENERIC
ReviewDISQUALIFIED
Anchor typeFINAL_ANDA
Anchor date2013-07-26
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2013-07-26
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
102386202027-05-18U U-620———
———
106536622027-05-18U U-620———
———
120830902027-05-18U U-620———
———
94864372027-05-18U U-620———
———
98616072027-05-18U U-620———
———
106536602027-07-20U U-620———
———
111100742027-07-20U U-620———
———
95728142027-07-20U U-620———
———
79153072027-08-24U U-620———
———
112349542028-01-18U U-620———
———
105488712028-04-11U U-620———
———
110969202028-04-11U U-620———
———
99077802028-04-11DP ————
———
91078982028-05-01U U-620———
———
95329712029-06-01DP ————
———
85132992030-09-07U U-620———
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
No exclusivity facts are recorded in this product snapshot.

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

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
201951 / 001FINAL_APPROVAL · FINAL_APPROVED2013-07-26—ACTAVIS ELIZABETH LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
202337 / 001FINAL_APPROVAL · FINAL_APPROVED2016-01-20—RK PHARMA INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
202510 / 001FINAL_APPROVAL · FINAL_APPROVED2020-07-24—STRIDES PHARMA INTERNATIONAL AGNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
214823 / 001FINAL_APPROVAL · FINAL_APPROVED2023-04-03—MSN LABORATORIES PRIVATE LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
202761 / 001FINAL_APPROVAL · FINAL_APPROVED2023-08-16—ZYDUS LIFESCIENCES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218564 / 001FINAL_APPROVAL · FINAL_APPROVED2024-07-01—AJANTA PHARMA LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
216041 / 001FINAL_APPROVAL · FINAL_APPROVED2024-07-25—AUROBINDO PHARMA LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
219058 / 001FINAL_APPROVAL · FINAL_APPROVED2025-08-06—TARO PHARMACEUTICAL INDUSTRIES LTDNEXACT_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 8 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
201951 / 001ACTAVIS ELIZABETH LLCFINAL_APPROVAL · FINAL_APPROVED2013-07-26 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
202337 / 001RK PHARMA INCFINAL_APPROVAL · FINAL_APPROVED2016-01-20 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
202510 / 001STRIDES PHARMA INTERNATIONAL AGFINAL_APPROVAL · FINAL_APPROVED2020-07-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
214823 / 001MSN LABORATORIES PRIVATE LTDFINAL_APPROVAL · FINAL_APPROVED2023-04-03 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
202761 / 001ZYDUS LIFESCIENCES LTDFINAL_APPROVAL · FINAL_APPROVED2023-08-16 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218564 / 001AJANTA PHARMA LTDFINAL_APPROVAL · FINAL_APPROVED2024-07-01 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
216041 / 001AUROBINDO PHARMA LTDFINAL_APPROVAL · FINAL_APPROVED2024-07-25 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
219058 / 001TARO PHARMACEUTICAL INDUSTRIES LTDFINAL_APPROVAL · FINAL_APPROVED2025-08-06 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (1)
TypeDateRoleBasisSource
GENERIC2013-07-26TERMINAL_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.