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Product profile · United States

DORYX

 ·  Patent Litigation & Settlement History ↓

IngredientDOXYCYCLINE HYCLATE
Application typeNDA
Application050795
Product005
Dosage formTABLET, DELAYED RELEASE
RouteORAL
StrengthEQ 200MG BASE
Approval date2013-04-11
Marketing statusDiscontinued
Status event—
ApplicantMAYNE PHARMA
Product source

Current GenericRadar decision

Year—
SelectionEXISTING_GENERIC
ReviewCOMPLETED
Anchor type—
Anchor date—
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2016-05-19
Status event—

ANDA 090431/005 Final 2016-05-19; FDA RLD brand source candidate. Earliest exact-product Final ANDA and explicit product correspondence still require independent confirmation.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
87157242028-02-03DP ————
———

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
090431 / 005FINAL_APPROVAL · FINAL_APPROVED2016-05-19—RISING PHARMA HOLDING INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
207494 / 002FINAL_APPROVAL · FINAL_APPROVED2016-11-15—PRINSTON PHARMACEUTICAL INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
090134 / 004FINAL_APPROVAL · FINAL_APPROVED2018-05-22—ACTAVIS ELIZABETH LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
200856 / 004FINAL_APPROVAL · FINAL_APPROVED2018-11-13—HERITAGE PHARMACEUTICALS INC DBA AVET PHARMACEUTICALS INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
213075 / 004FINAL_APPROVAL · FINAL_APPROVED2022-01-03—ALEMBIC PHARMACEUTICALS LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
208741 / 008FINAL_APPROVAL · FINAL_APPROVED2023-08-11—LUPIN 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 6 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
090431 / 005RISING PHARMA HOLDING INCFINAL_APPROVAL · FINAL_APPROVED2016-05-19 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
207494 / 002PRINSTON PHARMACEUTICAL INCFINAL_APPROVAL · FINAL_APPROVED2016-11-15 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
090134 / 004ACTAVIS ELIZABETH LLCFINAL_APPROVAL · FINAL_APPROVED2018-05-22 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
200856 / 004HERITAGE PHARMACEUTICALS INC DBA AVET PHARMACEUTICALS INCFINAL_APPROVAL · FINAL_APPROVED2018-11-13 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
213075 / 004ALEMBIC PHARMACEUTICALS LTDFINAL_APPROVAL · FINAL_APPROVED2022-01-03 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
208741 / 008LUPIN INCFINAL_APPROVAL · FINAL_APPROVED2023-08-11 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
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.