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

ENSTILAR

 ·  Patent Litigation & Settlement History ↓

IngredientBETAMETHASONE DIPROPIONATE; CALCIPOTRIENE
Application typeNDA
Application207589
Product001
Dosage formAEROSOL, FOAM
RouteTOPICAL
Strength0.064%;0.005%
Approval date2015-10-16
Marketing statusPrescription
Status event—
ApplicantLEO PHARMA AS
Product source

Current GenericRadar decision

Year—
SelectionEXISTING_GENERIC
ReviewCOMPLETED
Anchor type—
Anchor date—
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2023-03-21
Status event—

ANDA 214688/001 Final 2023-03-21; FDA RLD brand source candidate. Earliest exact-product Final ANDA and explicit product correspondence still require independent confirmation.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
101306402031-06-10DP ————
———
106176982031-06-10DP ————
———
106609082031-06-10DP/U U-2627———
———
106823642031-06-10DP ————
———
106881082031-06-10U U-2627———
———
107167992031-06-10DP ————
———
91197812031-06-10DP/U U-2627———
———
91197812031-06-10DP/U U-1761———
———
95662862031-06-10DP ————
———
101306402031-12-10— ————
—2031-12-10—
91197812031-12-10— ————
—2031-12-10—

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
214688 / 001FINAL_APPROVAL · FINAL_APPROVED2023-03-21—GLENMARK PHARMACEUTICALS 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 1 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
214688 / 001GLENMARK PHARMACEUTICALS LTDFINAL_APPROVAL · FINAL_APPROVED2023-03-21 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
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.