Data updated: Mar 10, 2026
NOCDURNA
DESMOPRESSIN ACETATE
Approved 2018-06-21
1
Indication
--
Phase 3 Trials
7
Years on Market
Details
- Status
- Discontinued
- First Approved
- 2018-06-21
- Routes
- SUBLINGUAL
- Dosage Forms
- TABLET
NOCDURNA Approval History
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What NOCDURNA Treats
1 FDA approvalsOriginally approved for its first indication in 2018 .
- Other (1)
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Pro Active Pipeline
Ongoing clinical trials by development phase
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Pro Key Completed Trials
Completed studies with published results, ranked by significance
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Trial Timeline
Full development history with FDA approval milestones
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Understanding FDA Approval Types
| Count | Type | What it means |
|---|---|---|
| - | ORIG | Original approval - drug first enters market |
| - | SUPPL - Efficacy | New indication (new disease/condition approved) |
| - | SUPPL - Labeling | Label text changes (warnings, dosing updates) |
| - | SUPPL - Manufacturing | Production changes (new facility) |
| - | SUPPL - Chemistry | Formulation changes (new dosage strength) |
Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.
NOCDURNA FDA Label Details
ProNOCDURNA Patents & Exclusivity
Latest Patent: Apr 2030
Patents (12 active)
US9974826
Expires Apr 13, 2030
US11963995
Expires May 21, 2029
US10137167
Expires May 21, 2029
US11020448
Expires May 21, 2029
+ 2 more patents
Source: FDA Orange Book
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Data Sources
Data sourced from official FDA and NIH databases. Click links to verify on original sources.