XADAGO
· Patent Litigation & Settlement History ↓
Current GenericRadar decision
Exact product/strength Final ANDA confirmed. Date is earliest verified official product approval for the batch. AG and tentative excluded. Approval date is not commercial launch date. No DS classification asserted.
Patent estate
Regulatory exclusivity
| Code | Start date | End date | Scope | Entire product | All indications | Full coverage date | Combination | Source |
|---|---|---|---|---|---|---|---|---|
| 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 / product | Event | Final date | Tentative date | Applicant | Authorized generic | Exact mapping | Source |
|---|---|---|---|---|---|---|---|
| 215902 / 001 | FINAL_APPROVAL · FINAL_APPROVED | 2023-06-14 | — | AUROBINDO PHARMA LTD | N | EXACT_PRODUCT · PENDING_PRODUCT_MAPPING | Source |
| 215739 / 001 | FINAL_APPROVAL · FINAL_APPROVED | 2024-04-25 | — | PRINSTON PHARMACEUTICAL INC | N | EXACT_PRODUCT · PENDING_PRODUCT_MAPPING | Source |
| 215978 / 001 | FINAL_APPROVAL · FINAL_APPROVED | 2024-12-31 | — | MSN LABORATORIES PRIVATE LTD | N | EXACT_PRODUCT · PENDING_PRODUCT_MAPPING | Source |
| 215913 / 001 | FINAL_APPROVAL · FINAL_APPROVED | 2025-06-13 | — | ZENARA PHARMA PRIVATE LTD | N | EXACT_PRODUCT · PENDING_PRODUCT_MAPPING | Source |
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 4 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 |
|---|---|---|---|---|---|---|
| 215902 / 001 | AUROBINDO PHARMA LTD | FINAL_APPROVAL · FINAL_APPROVED | 2023-06-14 | EXACT_PRODUCT · PENDING_PRODUCT_MAPPING | Source | — |
| 215739 / 001 | PRINSTON PHARMACEUTICAL INC | FINAL_APPROVAL · FINAL_APPROVED | 2024-04-25 | EXACT_PRODUCT · PENDING_PRODUCT_MAPPING | Source | — |
| 215978 / 001 | MSN LABORATORIES PRIVATE LTD | FINAL_APPROVAL · FINAL_APPROVED | 2024-12-31 | EXACT_PRODUCT · PENDING_PRODUCT_MAPPING | Source | — |
| 215913 / 001 | ZENARA PHARMA PRIVATE LTD | FINAL_APPROVAL · FINAL_APPROVED | 2025-06-13 | EXACT_PRODUCT · PENDING_PRODUCT_MAPPING | Source | — |
Decision evidence (1)
| Type | Date | Role | Basis | Source |
|---|---|---|---|---|
| GENERIC | 2023-06-14 | TERMINAL_GENERIC_BASIS | Exact product/strength Final ANDA confirmed. Date is earliest verified official product approval for the batch. AG and tentative excluded. Approval date is not commercial launch date. No DS classification asserted. | 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.
| Event date | Party | Event | Licensed entry | Evidence | Source |
|---|---|---|---|---|---|
| Not disclosed | Generic manufacturers named in private settlement agreements (individual parties not specified in this source) | SETTLEMENT Brand-level record; strength scope not established
|
2027-12-01 | SOURCE_CONFIRMED | Source |
| Newron 2025 Annual Report: US generic safinamide launch is not permitted before 2027-12-01 under settlement agreements. Supernus 2025 Form 10-K: sales may begin December 2027 or sooner under specified conditions. This is a contractual entry threshold, not a verified commercial launch. Brand-level record: do not infer a separate strength-specific licence, individual generic applicant, or actual launch. | |||||