This application view consolidates identifiers, linked product and market authorization context, dossier structure, sequence history, and active authority obligations in one place. Regulatory teams use it to understand readiness and risk before publishing new sequences or responding to open questions. Cross-links to labeling and variations maintain lifecycle traceability for post-approval changes. Inspection readiness risk is calculated from overdue commitments, failed sequences, and unresolved high-risk correspondence for immediate action.

Application ID
APP-061
Application Number
FDA-2024-0061
Procedure Type
NDA
Status
Active
Linked Product
Market Authorization
United States · FDA
Dossier Structure View
DossierFormatVersionModulesModule BreakdownStatus
DOS-061NeeS5.4.25M1 (11), M2 (9), M3 (7), M4 (5), M5 (12)Pending
Sequence Timeline
2023-06-30
0061 · Type IA Variation
Status: draft. ACK: pending.
2024-04-02
0161 · Renewal
Status: submitted. ACK: 2024-06-21.
2022-09-04
0261 · Initial Marketing Authorisation
Status: submitted. ACK: 2023-05-22.
2022-06-03
0361 · Safety Update
Status: pending. ACK: pending.
Open Questions and Commitments
CommitmentDue DatePriorityStatus
Implement Risk Minimisation Measures (RMM) per REMS requirements2025-03-15highIn Progress
Linked Labeling and Variations
Labeling ArtifactTypeVersionStatus
LBL-181IFU14.6Active
VariationTypeStatusSubmitted
FDA-2024-0061-V061MajorApproved2022-12-11
FDA-2024-0061-V161Type IBPending2023-06-10
FDA-2024-0061-V261MinorActive2022-09-12
FDA-2024-0061-V361MajorFailedpending
FDA-2024-0061-V461Type IAActive2024-02-09
Inspection Readiness Risk Panel
Risk Score: 1 · Overdue commitments: 0, failed/blocked sequences: 0, high-risk questions: 1.
Recommended next step: resolve outstanding questions and commitments before next publishing cycle to reduce inspection exposure.