TheraRadar
Data updated: May 26, 2026

NARDIL (phenelzine sulfate)

CNS Approved 1961-06-09

NARDIL is indicated for the treatment of Depression; Anxiety; Phobia.

Source: FDA Label • PARKE DAVIS

How NARDIL Works

Phenelzine is a potent, non-selective, and irreversible inhibitor of the enzyme monoamine oxidase (MAO). By inhibiting both MAO-A and MAO-B isoforms, the drug prevents the metabolic breakdown of monoamine neurotransmitters, including norepinephrine, serotonin, and dopamine. This leads to an accumulation of these neurotransmitters within the presynaptic neurons and an increase in their availability in the synaptic cleft, which is believed to be the primary mechanism for its antidepressant and anxiolytic effects.

1
Indication
--
Phase 3 Trials
64
Years on Market

Details

Status
Prescription
First Approved
1961-06-09
Routes
ORAL
Dosage Forms
TABLET

Companies

Active Ingredient: PHENELZINE SULFATE

NARDIL Approval History

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Original
New Indication
New Form
Label Update
14 FDA actions from 1961 to 2007
Aug 2007 SUPPL
Label · Labeling
Feb 2007 SUPPL
Mfg · Manufacturing (CMC)
Feb 2005 SUPPL
Label · Labeling

What NARDIL Treats

3 indications

NARDIL is approved for 3 conditions since its original approval in 1961. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Depression
  • Anxiety
  • Phobia
Source: FDA Label

NARDIL Boxed Warning

Suicidality and Antidepressant Drugs Antidepressants increased the risk compared to placebo of suicidal thinking and behavior (suicidality) in children, adolescents, and young adults in short-term studies of major depressive disorder (MDD) and other psychiatric disorders. Anyone considering the use of Nardil or any other antidepressant in a child, adolescent, or young adult must balance this risk with the clinical need. Short-term studies did not show an increase in the risk of suicidality with ...

NARDIL Competitive Set

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Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

Drugs Similar to NARDIL

3 of 19

FDA-approved drugs for similar conditions. Compare mechanisms and indications to understand treatment alternatives.

PHENELZINE SULFATE
PHENELZINE SULFATE
3 shared
NOVEL LABS INC
Shared indications:
DepressionAnxietyPhobia
AMOXAPINE
AMOXAPINE
2 shared
WATSON PHARMS TEVA
Shared indications:
DepressionAnxiety
OXAZEPAM
OXAZEPAM
2 shared
Teva
Shared indications:
AnxietyDepression
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Clinical Trial Registry

4 trials
Trial Sponsor ID Phase Status Title
NCT02217709 4P-14-1 NCI-2014-01791, HS-14-00331 Ph 2 completed Phenelzine Sulfate in Treating Patients With Non-metastatic Recurrent Prostate Cancer
NCT03979820 results posted 1386.16 2018-003965-32 Ph 1 terminated A Study in Healthy People to Test How Combining BI 1467335 and Tyramine Affects Blood Pressure
NCT03505528 Epi-PRIMED EpiAxis 001-0716 Ph 1 completed An Early Phase Study of Abraxane Combined With Phenelzine Sulfate in Patients With Metastatic or Advanced Breast Cancer
NCT01253642 results posted IRB00005688 NCI-2010-02037, SOL-09105-LM Ph 2 terminated Phenelzine Sulfate and Docetaxel in Treating Patients With Prostate Cancer With Progressive Disease After First-Line Therapy With Docetaxel
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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

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.

NARDIL FDA Label Details

Indications & Usage

FDA Label (PDF)

NARDIL is indicated for the treatment of Depression; Anxiety; Phobia.

⚠️ BOXED WARNING

Suicidality and Antidepressant Drugs Antidepressants increased the risk compared to placebo of suicidal thinking and behavior (suicidality) in children, adolescents, and young adults in short-term studies of major depressive disorder (MDD) and other psychiatric disorders. Anyone considering the use ...

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Data Sources

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