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Product profile · United States

SDAMLO

 ·  Patent Litigation & Settlement History ↓

IngredientAMLODIPINE BESYLATE
Application typeNDA
Application219531
Product001
Dosage formFOR SOLUTION
RouteORAL
StrengthEQ 2.5MG BASE/BOT
Approval date2025-07-24
Marketing statusPrescription
Status event—
ApplicantBRILLIAN PHARMA
Product source

Current GenericRadar decision

Year2007
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeTRUE_DS_PATENT
Anchor date2007-01-31
Patent anchor2007-01-31
Exclusivity anchor—
Protection date2007-07-08
First Final ANDA—
Status event—

Post-anchor patent or partial-scope exclusivity risk retained for Deep Review.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
US45729092007-01-31HISTORICAL_REFERENCE_NOT_EXACT_OB —YNTRUE_DS
Original dihydropyridine compound and permitted acid-addition salts. Historical FDA dates: PTE 2006-07-31 and PED 2007-01-31.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
NPP2004-01-082007-01-08Hypertension in children aged 6 to 17 years, included in the SDAMLO label. This partial scope does not cover adult angina and coronary artery disease.NN——Source
PED2007-01-082007-07-08Hypertension in children aged 6 to 17 years, included in the SDAMLO label. This partial scope does not cover adult angina and coronary artery disease.NN——Source

2026-10-13 · HISTORICAL_RECORDS_RECOVERED · Historical coverage: ANNUALS_AND_MONTHLY_REVIEWED

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

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
No generic approval facts are linked to this product.

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 0 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
No final-approval records are linked to this product.
Decision evidence (4)
TypeDateRoleBasisSource
PATENT2007-01-31CANONICAL_ANCHOROriginal dihydropyridine compound and permitted acid-addition salts. Historical FDA dates: PTE 2006-07-31 and PED 2007-01-31.Source
REGULATORY_EXCLUSIVITY—SCOPE_CONTEXTHypertension in children aged 6 to 17 years, included in the SDAMLO label. This partial scope does not cover adult angina and coronary artery disease.Source
REGULATORY_EXCLUSIVITY—SCOPE_CONTEXTHypertension in children aged 6 to 17 years, included in the SDAMLO label. This partial scope does not cover adult angina and coronary artery disease.Source
REGULATORY_STATUS2007-01-31CANONICAL_DECISIONPost-anchor patent or partial-scope exclusivity risk retained for Deep Review.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.