ZEMDRI
· Patent Litigation & Settlement History ↓
Current GenericRadar decision
FDA_OB_DISC_ACTION_MONTH; canonical=2032-06-25; exact Final ANDA not directly identified; not generic absence; FDA DISC 2026-05
Patent estate
| Patent | Effective date | Official listing | TRUE_DS | DS grade | Claim classification / basis | PTE | PED | Family |
|---|---|---|---|---|---|---|---|---|
| 8822424 | 2028-11-21 | DP — | N | N | DP | B1C0201 issued-claim review2026-10-14: DP | — | — | — |
| 8822424 | 2028-11-21 | ORANGE_BOOK — | N | N | DP English description not available. | — | — | — |
| 9266919 | 2028-11-21 | U U-2328 | N | Y | U | B1C0201 issued-claim review2026-10-14: U | — | — | — |
| 9266919 | 2028-11-21 | ORANGE_BOOK U-2328 | N | Y | U English description not available. | — | — | — |
| 9688711 | 2028-11-21 | DS/U U-2328 | Y | N | TRUE_DS | B1C0201 issued-claim review2026-10-14: TRUE_DS | — | — | — |
| 9688711 | 2028-11-21 | ORANGE_BOOK U-2328 | Y | N | TRUE_DS English description not available. | — | — | — |
| 8383596 | 2032-06-25 | DS/U U-2328 | Y | N | TRUE_DS | B1C0201 issued-claim review2026-10-14: TRUE_DS | — | — | — |
| 8383596 | 2032-06-25 | ORANGE_BOOK U-2328 | Y | N | TRUE_DS English description not available. | — | — | — |
Regulatory exclusivity
| Code | Start date | End date | Scope | Entire product | All indications | Full coverage date | Combination | Source |
|---|---|---|---|---|---|---|---|---|
| NCE | 2018-06-25 | 2023-06-25 | English description not available. | Y | Y | 2023-06-25 | — | Source |
| NCE | 2018-06-25 | 2023-06-25 | English description not available. | Y | Y | 2023-06-25 | Source | |
| GAIN | 2023-06-25 | 2028-06-25 | English description not available. | Y | Y | 2028-06-25 | — | Source |
| GAIN | 2023-06-25 | 2028-06-25 | English description not available. | Y | Y | 2028-06-25 | Source |
2026-10-10 · CURRENT_SOURCE_RECORDS_FOUND · Historical coverage: NOT_COMPLETE
Generic approval evidence
| Application / product | Event | Final date | Tentative date | Applicant | Authorized generic | Exact mapping | Source |
|---|---|---|---|---|---|---|---|
| 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.
| API | Holder / manufacturer | Holder country | Filing type | Number | Status | Filed date | Available for reference | Source | Last 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 / product | Applicant | Event / status | First marketed | Product mapping | Source | Last 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 / product | Applicant | Event / status | Tentative date | Follow-up final approval | Product mapping | Source | Last 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 / product | Applicant | Event / status | Certification event date | Product mapping | Source | Last 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 / product | Applicant | Event / status | Final approval date | Product mapping | Source | Last verified |
|---|---|---|---|---|---|---|
| No final-approval records are linked to this product. | ||||||
Decision evidence (7)
| Type | Date | Role | Basis | Source |
|---|---|---|---|---|
| PATENT | 2028-11-21 | HISTORICAL_CONTEXT | English description not available. | Source |
| PATENT | 2028-11-21 | HISTORICAL_CONTEXT | English description not available. | Source |
| PATENT | 2028-11-21 | HISTORICAL_CONTEXT | English description not available. | Source |
| PATENT | 2032-06-25 | HISTORICAL_CONTEXT | English description not available. | Source |
| REGULATORY_EXCLUSIVITY | — | HISTORICAL_CONTEXT | English description not available. | Source |
| REGULATORY_EXCLUSIVITY | — | HISTORICAL_CONTEXT | English description not available. | Source |
| REGULATORY_STATUS | — | TERMINAL_STATUS | FDA_OB_DISC_ACTION_MONTH; canonical=2032-06-25; exact Final ANDA not directly identified; not generic absence; FDA DISC 2026-05 | Source |
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.