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Product profile · United States

VOGELXO

 ·  Patent Litigation & Settlement History ↓

IngredientTESTOSTERONE
Application typeNDA
Application204399
Product003
Dosage formGEL, METERED
RouteTRANSDERMAL
Strength12.5MG/1.25GM ACTUATION
Approval date2014-06-04
Marketing statusPrescription
Status event—
ApplicantUPSHER SMITH LABS
Product source

Current GenericRadar decision

Year2014
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeAPPROVAL_YEAR_FALLBACK
Anchor date2014-06-04
Patent anchor—
Exclusivity anchor—
Protection date2034-02-11
First Final ANDA—
Status event—

No verified direct-reference Final ANDA or unrestricted TrueDS/DS-equivalent/full-coverage exclusivity anchor is established for this exact product. Apply the approval-year DR fallback under the review policy. VOGELXO is BX-rated in the current Orange Book. Matching AB1 testosterone-pump ANDAs cannot be assigned as therapeutically equivalent to VOGELXO; its formulation and reference identity are distinct. No direct-reference Final ANDA is established.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
87854262034-02-11DP/U U-1531NNTESTOSTERONE_TRANSDERMAL_GEL
———
87854262034-02-11DP/U U-1531NNTESTOSTERONE_TRANSDERMAL_GEL
Independent composition claims require testosterone, alcohol, a specified adipate/laurate/oleyl cosolvent system, a polyol system and gel-forming polymer with content limits.
———
92956752034-02-11DP/U U-1531NNTESTOSTERONE_TRANSDERMAL_GEL
———
92956752034-02-11DP/U U-1531NNTESTOSTERONE_TRANSDERMAL_GEL
Claim 1 requires a testosterone gel with specified alcohol, adipate/laurate/oleyl cosolvents, polyols, polymer and water. It is not a compound claim.
———
96623402034-02-11DP/U U-1531NNTESTOSTERONE_GEL_TREATMENT
———
96623402034-02-11DP/U U-1531NNTESTOSTERONE_GEL_TREATMENT
Claim 1 treats hypogonadism using a gel with defined testosterone, alcohol, cosolvent/polyol and polymer restrictions. Coverage of the therapeutic condition does not remove formulation limits.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
No exclusivity facts are recorded in this product snapshot.

2026-10-11 · CURRENT_SNAPSHOT_NO_RECORD · Historical coverage: NOT_COMPLETE

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

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
076737 / 003FINAL_APPROVAL · FINAL_APPROVED2015-03-09—ACTAVIS LABORATORIES UT INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
212984 / 002FINAL_APPROVAL · FINAL_APPROVED2024-02-09—ENCUBE ETHICALS PRIVATE 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 2 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
076737 / 003ACTAVIS LABORATORIES UT INCFINAL_APPROVAL · FINAL_APPROVED2015-03-09 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
212984 / 002ENCUBE ETHICALS PRIVATE LTDFINAL_APPROVAL · FINAL_APPROVED2024-02-09 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (4)
TypeDateRoleBasisSource
PATENT2034-02-11FTO_TAILClaim 1 treats hypogonadism using a gel with defined testosterone, alcohol, cosolvent/polyol and polymer restrictions. Coverage of the therapeutic condition does not remove formulation limits.Source
PATENT2034-02-11FTO_TAILIndependent composition claims require testosterone, alcohol, a specified adipate/laurate/oleyl cosolvent system, a polyol system and gel-forming polymer with content limits.Source
PATENT2034-02-11FTO_TAILClaim 1 requires a testosterone gel with specified alcohol, adipate/laurate/oleyl cosolvents, polyols, polymer and water. It is not a compound claim.Source
REGULATORY_STATUS2014-06-04DECISION_BASISNo verified direct-reference Final ANDA or unrestricted TrueDS/DS-equivalent/full-coverage exclusivity anchor is established for this exact product. Apply the approval-year DR fallback under the review policy. VOGELXO is BX-rated in the current Orange Book. Matching AB1 testosterone-pump ANDAs cannot be assigned as therapeutically equivalent to VOGELXO; its formulation and reference identity are distinct. No direct-reference Final ANDA is established.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.