TheraRadar

Pharma Intelligence, Simplified

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

Companies

Active Ingredient: DESMOPRESSIN ACETATE

NOCDURNA Approval History

Loading approval history...

What NOCDURNA Treats

1 FDA approvals

Originally approved for its first indication in 2018 .

  • Other (1)
๐Ÿ”ฌ

Active Pipeline

Pro

Ongoing clinical trials by development phase

Loading...
โญ

Key Completed Trials

Pro

Completed studies with published results, ranked by significance

Loading...
๐Ÿ“Š

Trial Timeline

Full development history with FDA approval milestones

Loading...
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

Pro

NOCDURNA 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

Want competitive intelligence?

See who's developing similar drugs and track their progress

View Pipeline Dashboard

Data Sources

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