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Product profile · United States

MOXIDECTIN

 ·  Patent Litigation & Settlement History ↓

IngredientMOXIDECTIN
Application typeNDA
Application210867
Product001
Dosage formTABLET
RouteORAL
Strength2MG
Approval date2018-06-13
Marketing statusPrescription
Status event—
ApplicantMDGH
Product source

Current GenericRadar decision

Year2025
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeREGULATORY_EXCLUSIVITY
Anchor date2025-06-13
Patent anchor—
Exclusivity anchor2025-06-13
Protection date2032-02-07
First Final ANDA—
Status event—

Original age-at-least-12 ODE to 2025-06-13 and pediatric 4-to-under-12 ODE to 2032-02-07 together cover the current population. Joint full-scope date is 2025-06-13; pediatric-only protection remains later. Veterinary combination/crystal/process rights are not unrestricted substance anchors.

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
GNR_FULL_SCOPE2018-06-132025-06-13Onchocerciasis, adults and children age at least 4 and weight at least 13 kg.YY2025-06-13Source
NPP—2028-02-07New patient population; not automatically full label.NN——Source
NPP2025-02-072028-02-07New patient population; not automatically full label.NN——Source
ODE-528—2032-02-07Onchocerciasis in children age 4 to under 12 and weight at least 13 kg.NN——Source
ODE-5282025-02-072032-02-07Onchocerciasis in children age 4 to under 12 and weight at least 13 kg.NN——Source

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

2026-10-10 · CURRENT_SOURCE_RECORDS_FOUND · 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
REGULATORY_EXCLUSIVITY—SCOPE_CONTEXTNew patient population; not automatically full label.Source
REGULATORY_EXCLUSIVITY—SCOPE_CONTEXTOnchocerciasis in children age 4 to under 12 and weight at least 13 kg.Source
REGULATORY_EXCLUSIVITY2025-06-13CANONICAL_ANCHOROnchocerciasis, adults and children age at least 4 and weight at least 13 kg.Source
REGULATORY_STATUS2025-06-13CANONICAL_DECISIONOriginal age-at-least-12 ODE to 2025-06-13 and pediatric 4-to-under-12 ODE to 2032-02-07 together cover the current population. Joint full-scope date is 2025-06-13; pediatric-only protection remains later. Veterinary combination/crystal/process rights are not unrestricted substance anchors.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.