TheraRadar
Data updated: May 26, 2026

NOCDURNA (desmopressin acetate)

Rare Disease Approved 2018-06-21
Jump to: Indications Approvals Trials Competitors Safety Patents
1
Indication
--
Phase 3 Trials
7
Years on Market

Details

Status
Discontinued
First Approved
2018-06-21
Patent Cliff
2030

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Patent cliff and revenue data

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Routes
SUBLINGUAL
Dosage Forms
TABLET

Companies

FERRING PHARMS INC
Active Ingredient: DESMOPRESSIN ACETATE

NOCDURNA Approval History

2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
2 FDA actions from 2018 to 2018
Jun 2018 ORIGINAL
Update · Type 5 - New Formulation or New Manufacturer
FDA Letter Label

What NOCDURNA Treats

1 FDA approvals

Originally approved for its first indication in 2018 .

  • Other (1)
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

ClinicalTrials.gov ↗ Pro

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

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4 OB patents · 3 families · 116 international docs across 19 countries

NOCDURNA Patents & Exclusivity

Latest Patent: Apr 2030

Patents (4 active)

US9974826 Expires Apr 13, 2030
US11963995 Expires May 21, 2029
US10137167 Expires May 21, 2029
US11020448 Expires May 21, 2029
Source: FDA Orange Book

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Revenue Insights

  • • Quarterly revenue tracking
  • • Historical trend analysis

Patent Timeline

  • • Cliff: 2030
  • • 12 active patents

Trial Analysis

  • • Clinical trial tracking
  • • Development stage analysis

Competitive Landscape

  • • Competitor tracking
  • • Same target/indication analysis
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Data Sources

FDA Approval: NDA022517 → Patents: FDA Orange Book → Trials: ClinicalTrials.gov →

Data sourced from official FDA and NIH databases. Click links to verify on original sources.