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IngredientDORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE
Application typeNDA
Application202667
Product001
Dosage formSOLUTION/DROPS
RouteOPHTHALMIC
StrengthEQ 2% BASE;EQ 0.5% BASE
Approval date2012-02-01
Marketing statusPrescription
Status event—
ApplicantTHEA PHARMA
Product source

Current GenericRadar decision

Year2018
SelectionEXISTING_GENERIC
ReviewDISQUALIFIED
Anchor typeFINAL_ANDA
Anchor date2018-07-24
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2018-07-24
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
No patent facts are recorded for this product.

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
077847 / 001FINAL_APPROVAL · FINAL_APPROVED2008-10-28—HIKMA PHARMACEUTICALS USA INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
078201 / 001FINAL_APPROVAL · FINAL_APPROVED2008-10-28—RUBICON RESEARCH LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
078749 / 001FINAL_APPROVAL · FINAL_APPROVED2008-11-06—SANDOZ INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
090037 / 001FINAL_APPROVAL · FINAL_APPROVED2009-07-14—BAUSCH AND LOMB INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
078704 / 001FINAL_APPROVAL · FINAL_APPROVED2009-09-28—TEVA PHARMACEUTICALS USANEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
090604 / 001FINAL_APPROVAL · FINAL_APPROVED2009-11-18—SANDOZ INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
091180 / 001FINAL_APPROVAL · FINAL_APPROVED2013-12-04—ZAMBON SPANEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
202054 / 001FINAL_APPROVAL · FINAL_APPROVED2014-09-03—REGCON HOLDINGS LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
203058 / 001FINAL_APPROVAL · FINAL_APPROVED2014-09-22—EPIC PHARMA LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
201998 / 001FINAL_APPROVAL · FINAL_APPROVED2014-12-17—CHARTWELL MOLECULAR HOLDINGS LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
207630 / 001FINAL_APPROVAL · FINAL_APPROVED2018-07-24—EUGIA PHARMA SPECIALITIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
205295 / 001FINAL_APPROVAL · FINAL_APPROVED2019-06-13—FDC LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
207523 / 001FINAL_APPROVAL · FINAL_APPROVED2019-06-25—SOMERSET THERAPEUTICS LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
204777 / 001FINAL_APPROVAL · FINAL_APPROVED2020-05-28—MICRO LABS LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
213099 / 001FINAL_APPROVAL · FINAL_APPROVED2021-05-04—ALEMBIC PHARMACEUTICALS LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
207629 / 001FINAL_APPROVAL · FINAL_APPROVED2021-05-14—EUGIA PHARMA SPECIALITIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
215936 / 001FINAL_APPROVAL · FINAL_APPROVED2022-01-25—MICRO LABS LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
215520 / 001FINAL_APPROVAL · FINAL_APPROVED2022-09-19—GLAND PHARMA LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
217260 / 001FINAL_APPROVAL · FINAL_APPROVED2023-05-01—INGENUS PHARMACEUTICALS LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
216308 / 001FINAL_APPROVAL · FINAL_APPROVED2025-02-18—ALEMBIC THERAPEUTICS LLCNEXACT_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 20 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
077847 / 001HIKMA PHARMACEUTICALS USA INCFINAL_APPROVAL · FINAL_APPROVED2008-10-28 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
078201 / 001RUBICON RESEARCH LTDFINAL_APPROVAL · FINAL_APPROVED2008-10-28 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
078749 / 001SANDOZ INCFINAL_APPROVAL · FINAL_APPROVED2008-11-06 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
090037 / 001BAUSCH AND LOMB INCFINAL_APPROVAL · FINAL_APPROVED2009-07-14 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
078704 / 001TEVA PHARMACEUTICALS USAFINAL_APPROVAL · FINAL_APPROVED2009-09-28 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
090604 / 001SANDOZ INCFINAL_APPROVAL · FINAL_APPROVED2009-11-18 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
091180 / 001ZAMBON SPAFINAL_APPROVAL · FINAL_APPROVED2013-12-04 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
202054 / 001REGCON HOLDINGS LLCFINAL_APPROVAL · FINAL_APPROVED2014-09-03 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
203058 / 001EPIC PHARMA LLCFINAL_APPROVAL · FINAL_APPROVED2014-09-22 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
201998 / 001CHARTWELL MOLECULAR HOLDINGS LLCFINAL_APPROVAL · FINAL_APPROVED2014-12-17 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
207630 / 001EUGIA PHARMA SPECIALITIES LTDFINAL_APPROVAL · FINAL_APPROVED2018-07-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
205295 / 001FDC LTDFINAL_APPROVAL · FINAL_APPROVED2019-06-13 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
207523 / 001SOMERSET THERAPEUTICS LLCFINAL_APPROVAL · FINAL_APPROVED2019-06-25 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
204777 / 001MICRO LABS LTDFINAL_APPROVAL · FINAL_APPROVED2020-05-28 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
213099 / 001ALEMBIC PHARMACEUTICALS LTDFINAL_APPROVAL · FINAL_APPROVED2021-05-04 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
207629 / 001EUGIA PHARMA SPECIALITIES LTDFINAL_APPROVAL · FINAL_APPROVED2021-05-14 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
215936 / 001MICRO LABS LTDFINAL_APPROVAL · FINAL_APPROVED2022-01-25 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
215520 / 001GLAND PHARMA LTDFINAL_APPROVAL · FINAL_APPROVED2022-09-19 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
217260 / 001INGENUS PHARMACEUTICALS LLCFINAL_APPROVAL · FINAL_APPROVED2023-05-01 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
216308 / 001ALEMBIC THERAPEUTICS LLCFINAL_APPROVAL · FINAL_APPROVED2025-02-18 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (1)
TypeDateRoleBasisSource
GENERIC2018-07-24TERMINAL_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.