DOXEPIN HYDROCHLORIDE
Details
- Status
- Prescription
- First Approved
- 1972-01-31
- Routes
- ORAL, TOPICAL
- Dosage Forms
- TABLET, CAPSULE, CONCENTRATE, CREAM
Companies
DOXEPIN HYDROCHLORIDE Approval History
What DOXEPIN HYDROCHLORIDE Treats
1 indicationsDOXEPIN HYDROCHLORIDE is approved for 1 conditions since its original approval in 1972. These indications span multiple therapeutic areas including oncology, immunology, and more.
- Insomnia
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Active Pipeline
Ongoing clinical trials by development phase
Key Completed Trials
Completed studies with published results, ranked by significance
Trial Timeline
Full development history with FDA approval milestones
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.
DOXEPIN HYDROCHLORIDE FDA Label Details
ProIndications & Usage
FDA Label (PDF)Doxepin tablets are indicated for the treatment of insomnia characterized by difficulty with sleep maintenance. The clinical trials performed in support of efficacy were up to 3 months in duration. Doxepin tablets are indicated for the treatment of insomnia characterized by difficulties with sleep maintenance.
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Data Sources
Data sourced from official FDA and NIH databases. Click links to verify on original sources.