Market LIVE
Published markets; coverage varies by country
Product profile · United States

ORAVIG

 ·  Patent Litigation & Settlement History ↓

IngredientMICONAZOLE
Application typeNDA
Application022404
Product001
Dosage formTABLET
RouteBUCCAL
Strength50MG
Approval date2010-04-16
Marketing statusPrescription
Status event—
ApplicantGALT PHARMS
Product source

Current GenericRadar decision

Year2013
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeREGULATORY_EXCLUSIVITY
Anchor date2013-04-16
Patent anchor—
Exclusivity anchor2013-04-16
Protection date2022-09-11
First Final ANDA—
Status event—

POST_ANCHOR_RIGHTS. Canonical anchor 2013-04-16; tails [{"kind":"PATENT","number_or_code":"US6916485","date":"2022-09-11"},{"kind":"PATENT","number_or_code":"US7651698","date":"2022-09-11"},{"kind":"PATENT","number_or_code":"US8518442","date":"2022-09-11"}]

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
US69164852022-09-11DP/U U-1051NNDP
Product formulation, delivery, excipient, release or preparation claims; no broad independent active-compound claim established. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.
———
US76516982022-09-11U U-1051NNDP_U
Buccal candidiasis treatment using a quantitatively specified bioadhesive system; indication correspondence does not establish every formulation and dissolution limitation. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.
———
US85184422022-09-11DP —NNDP
Product formulation, delivery, excipient, release or preparation claims; no broad independent active-compound claim established. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
NDF2010-04-162013-04-16Original new dosage form, new combination or exact new product approval; covers its approved formulation/use scope at this original approval.YY2013-04-16Source

2026-10-12 · HISTORICAL_RECORDS_RECOVERED · Historical coverage: ANNUALS_2011_2026_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 (5)
TypeDateRoleBasisSource
PATENT2022-09-11FTO_TAILProduct formulation, delivery, excipient, release or preparation claims; no broad independent active-compound claim established. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.Source
PATENT2022-09-11FTO_TAILProduct formulation, delivery, excipient, release or preparation claims; no broad independent active-compound claim established. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.Source
PATENT2022-09-11FTO_TAILBuccal candidiasis treatment using a quantitatively specified bioadhesive system; indication correspondence does not establish every formulation and dissolution limitation. Full product scope is not established by the retrieved claims and product evidence; no DS-equivalent promotion is made.Source
REGULATORY_EXCLUSIVITY2013-04-16CANONICAL_ANCHOROriginal new dosage form, new combination or exact new product approval; covers its approved formulation/use scope at this original approval.Source
REGULATORY_STATUS2013-04-16DECISION_BASISPOST_ANCHOR_RIGHTS. Canonical anchor 2013-04-16; tails [{"kind":"PATENT","number_or_code":"US6916485","date":"2022-09-11"},{"kind":"PATENT","number_or_code":"US7651698","date":"2022-09-11"},{"kind":"PATENT","number_or_code":"US8518442","date":"2022-09-11"}]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.