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Molecule

Phenelzine

Also known as phenelzine sulfate
Available on requestPsychiatry
Presentations
2
Brands
1
Manufacturers
1
Available from stock
0

Phenelzine is a monoamine oxidase inhibitor. It is available as tablets for oral use. MedsAcross supplies Phenelzine for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
Monoamine Oxidase Inhibitor, Monoamine Oxidase Inhibitors
ATC classification
N06AF03 Phenelzine · Monoamine oxidase inhibitor
US FDA first approval
9 June 1961
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Oral
Dosage forms
Tablet
Identifiers
UNII O408N561GFRxCUI 8123CAS 51-71-8DrugBank DB00780Q1747559

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

NARDIL has been found to be effective in depressed patients clinically characterized as "atypical," "nonendogenous," or "neurotic." These patients often have mixed anxiety and depression and phobic or hypochondriacal features. There is less conclusive evidence of its usefulness with severely depressed patients with endogenous features. NARDIL should rarely be the first antidepressant drug used. Rather, it is more suitable for use with patients who have failed to respond to the drugs more commonly used for these conditions.

Source: US FDA prescribing information

Dosing overview

Initial dose The usual starting dose of NARDIL is one tablet (15 mg) three times a day. Early phase treatment Dosage should be increased to at least 60 mg per day at a fairly rapid pace consistent with patient tolerance. It may be necessary to increase dosage up to 90 mg per day to obtain sufficient MAO inhibition. Many patients do not show a clinical response until treatment at 60 mg has been continued for at least 4 weeks. Maintenance dose After maximum benefit from NARDIL is achieved, dosage should be reduced slowly over several weeks. Maintenance dose may be as low as one tablet, 15 mg, a day or every other day, and should be continued for as long as is required.

Source: US FDA prescribing information

Contraindications

NARDIL should not be used in patients who are hypersensitive to the drug or its ingredients, with pheochromocytoma, congestive heart failure, severe renal impairment or renal disease, a history of liver disease, or abnormal liver function tests. The potentiation of sympathomimetic substances and related compounds by MAO inhibitors may result in hypertensive crises. Therefore, patients being treated with NARDIL should not take sympathomimetic drugs (including amphetamines, cocaine, methylphenidate, dopamine, epinephrine, and norepinephrine) or related compounds (including methyldopa, L-dopa, L-tryptophan, L-tyrosine, and phenylalanine).

Source: US FDA prescribing information

Warnings and precautions

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. Clinical Worsening and Suicide Risk Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications, and this risk may persist until significant remission occurs.

Source: US FDA prescribing information

Side effects

NARDIL is a potent inhibitor of monoamine oxidase. Because this enzyme is widely distributed throughout the body, diverse pharmacologic effects can be expected to occur. When they occur, such effects tend to be mild or moderate in severity, often subside as treatment continues, and can be minimized by adjusting dosage, rarely is it necessary to institute counteracting measures or to discontinue NARDIL. Common side effects include: Nervous System —Dizziness, headache, drowsiness, sleep disturbances (including insomnia and hypersomnia), fatigue, weakness, tremors, twitching, myoclonic movements, hyperreflexia. Gastrointestin al—Constipation, dry mouth, gastrointestinal disturbances, elevated serum transaminases (without accompanying signs and symptoms). Metabolic —Weight gain. Cardiovascular —Postural hypotension, edema.

Source: US FDA prescribing information

Interactions

In patients receiving nonselective monoamine oxidase (MAO) inhibitors in combination with serotoninergic agents (e.g., dexfenfluramine, fluoxetine, fluvoxamine, paroxetine, sertraline, citalopram, venlafaxine) there have been reports of serious, sometimes fatal, reactions. Because NARDIL is a monoamine oxidase (MAO) inhibitor, NARDIL should not be used concomitantly with a serotoninergic agent. Administration of guanethidine to patients receiving an MAO inhibitor can produce moderate to severe hypertension due to release of catecholamines. At least two weeks should elapse between withdrawal of the MAO inhibitor and the initiation of guanethidine.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

2 presentations of Phenelzine, sorted by availability.

MedicineManufacturerRegisterAvailability
Phenelzine 15 mg tabletOralGeneric name—US FDAAvailable on request
Nardil 15 mg tabletOralParke-DavisUS FDAAvailable on request

Brands by market

1 brand names across 1 markets.

Brand names by country

United States

Manufacturers

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 9 June 1961Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Conditions

Conditions linked to Phenelzine in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Phenelzine available for export from India?

Yes, on request. MedsAcross lists 2 presentations of Phenelzine and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Phenelzine have?

The catalogue lists 1 brand names for Phenelzine, including Nardil.

Is Phenelzine approved by the US FDA?

Yes. The US FDA first approved Phenelzine on 9 June 1961, according to Drugs@FDA.

Does Phenelzine need cold chain shipping?

No listed presentation of Phenelzine is recorded as needing a cold chain. Storage conditions are shown on each presentation page.

Which ATC class is Phenelzine in?

Phenelzine is classified under ATC code N06AF03 (Phenelzine).

References

  1. Nardil prescribing information (Parke-Davis). U.S. National Library of Medicine, DailyMed. Retrieved 5 November 2026

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