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  1. pharmadog
  2. ›drugs
  3. ›Duloxetine Hydrochloride
drug
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duloxetine hydrochloride DR

Marketedupdated 3mo ago
by Qingdao Baheal Medical Inc
Approved
community read0 votes

🐶 often sniffed alongside

top 3
  • tagApproval24 co-mentions · 12 sources
  • drugDULOXETINE HYDROCHLORIDE12 co-mentions · 12 sources
  • tagSmall Molecule12 co-mentions · 12 sources

indications

investigational
Major Depression

all catalysts(12)

approval · 12
Jun 9, 2014
approval
12y ago
DULOXETINE HYDROCHLORIDE — FDA approval
duloxetine hydrochloride DR
→
Feb 8, 2024
approval
3y ago
DULOXETINE HYDROCHLORIDE — FDA approval
duloxetine hydrochloride DR
→
Feb 8, 2024
approval
3y ago
DULOXETINE HYDROCHLORIDE — FDA approval
duloxetine hydrochloride DR
→
Feb 8, 2024
approval
3y ago
DULOXETINE HYDROCHLORIDE — FDA approval
duloxetine hydrochloride DR
→
Feb 8, 2024
approval
3y ago
DULOXETINE HYDROCHLORIDE — FDA approval
duloxetine hydrochloride DR
→
Feb 8, 2024
approval
3y ago
DULOXETINE HYDROCHLORIDE — FDA approval
duloxetine hydrochloride DR
→
Feb 8, 2024
approval
3y ago
DULOXETINE HYDROCHLORIDE — FDA approval
duloxetine hydrochloride DR
→
Feb 8, 2024
approval
3y ago
DULOXETINE HYDROCHLORIDE — FDA approval
duloxetine hydrochloride DR
→
Feb 8, 2024
approval
3y ago
DULOXETINE HYDROCHLORIDE — FDA approval
duloxetine hydrochloride DR
→
Feb 8, 2024
approval
3y ago
DULOXETINE HYDROCHLORIDE — FDA approval
duloxetine hydrochloride DR
→
Feb 27, 2026
approval
6mo ago
DULOXETINE HYDROCHLORIDE — FDA approval
duloxetine hydrochloride DR
→
Apr 9, 2026
approval
4mo ago
DULOXETINE HYDROCHLORIDE — FDA approval
duloxetine hydrochloride DR
→
view all 12 catalysts →

Trials studying duloxetine hydrochloride DR

  • phase2A Phase II Study to Evaluate NH102 for Depressioncompletedn=243
  • phase3Efficacy and Safety Study of Levomilnacipran Hydrochloride Extended-Release Capsules in Major Depressive Disordercompletedn=392
  • phase2A Study of the Effectiveness and Safety of JS1-1-01 in Patients With Moderate to Severe Depressioncompletedn=267
  • —Duloxetine Compassionate Use in Patients Who Have Completed a Previous Neuroscience Duloxetine Clinical Trialapproved for marketing

Patent cliff

source: FDA Orange Book
first barrier falls
Apr 13, 2037
~10.7 years out

Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.

patents (20)

  • Apr 13, 2037formulationUS 10413525
  • Apr 13, 2037formulationUS 10413525
  • Apr 13, 2037formulationUS 10413525
  • Apr 13, 2037formulationUS 10413525
  • Apr 13, 2037formulationUS 10959982
  • Apr 13, 2037formulationUS 10959982
  • Apr 13, 2037formulationUS 10959982
  • Apr 13, 2037formulationUS 10959982
  • Apr 13, 2037formulationUS 11202772
  • Apr 13, 2037formulationUS 11202772
  • Apr 13, 2037formulationUS 11202772
  • Apr 13, 2037formulationUS 11202772
  • Apr 13, 2037formulationUS 12171742
  • Apr 13, 2037formulationUS 12171742
  • Apr 13, 2037formulationUS 12171742
  • Apr 13, 2037formulationUS 12171742
  • Apr 13, 2037formulationUS 9839626
  • Apr 13, 2037formulationUS 9839626
  • Apr 13, 2037formulationUS 9839626
  • Apr 13, 2037formulationUS 9839626

News(0)

no news has mentioned this drug yet

brand
Duloxetine Hydrochloride
generic
duloxetine hydrochloride
indication
Diabetic Neuropathic Pain
phase
marketed
Data sources
openFDA · ClinicalTrials.gov
last refreshed 1h ago
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