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Product profile · United States

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IngredientAMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
Application typeNDA
Application200175
Product004
Dosage formTABLET
RouteORAL
StrengthEQ 10MG BASE;12.5MG;40MG
Approval date2010-07-23
Marketing statusPrescription
Status event—
ApplicantCOSETTE
Product source

Current GenericRadar decision

Year2016
SelectionEXISTING_GENERIC
ReviewDISQUALIFIED
Anchor typeFINAL_ANDA
Anchor date2016-10-26
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2016-10-26
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
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
203580 / 004FINAL_APPROVAL · FINAL_APPROVED2016-10-26—TORRENT PHARMACEUTICALS LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
206137 / 004FINAL_APPROVAL · FINAL_APPROVED2016-10-26—PH HEALTH LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
202491 / 004FINAL_APPROVAL · FINAL_APPROVED2016-11-03—TEVA PHARMACEUTICALS USANEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
210718 / 004FINAL_APPROVAL · FINAL_APPROVED2025-05-14—PIRAMAL HEALTHCARE UK LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
207088 / 004FINAL_APPROVAL · FINAL_APPROVED2025-07-18—MACLEODS PHARMACEUTICALS LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
209242 / 004FINAL_APPROVAL · FINAL_APPROVED2025-10-06—HETERO LABS LTD UNIT VNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
207437 / 004FINAL_APPROVAL · FINAL_APPROVED2025-11-24—MICRO LABS 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 7 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
203580 / 004TORRENT PHARMACEUTICALS LTDFINAL_APPROVAL · FINAL_APPROVED2016-10-26 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
206137 / 004PH HEALTH LTDFINAL_APPROVAL · FINAL_APPROVED2016-10-26 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
202491 / 004TEVA PHARMACEUTICALS USAFINAL_APPROVAL · FINAL_APPROVED2016-11-03 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
210718 / 004PIRAMAL HEALTHCARE UK LTDFINAL_APPROVAL · FINAL_APPROVED2025-05-14 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
207088 / 004MACLEODS PHARMACEUTICALS LTDFINAL_APPROVAL · FINAL_APPROVED2025-07-18 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
209242 / 004HETERO LABS LTD UNIT VFINAL_APPROVAL · FINAL_APPROVED2025-10-06 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
207437 / 004MICRO LABS LTDFINAL_APPROVAL · FINAL_APPROVED2025-11-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (1)
TypeDateRoleBasisSource
GENERIC2016-10-26TERMINAL_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.