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Molecule

Phenoxybenzamine

Also known as phenoxybenzamine hydrochloride
Available on requestCardiology
Presentations
1
Brands
0
Manufacturers
0
Available from stock
0

Phenoxybenzamine is an alpha-adrenergic blocker indicated in the treatment of pheochromocytoma, to control episodes of hypertension and sweating. It is available as capsules for oral use. MedsAcross supplies Phenoxybenzamine 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
Alpha-Adrenergic Blocker, Adrenergic alpha-Antagonists
ATC classification
C04AX02 Phenoxybenzamine · Peripheral vasodilators, subgroup C04A, subgroup C04AX
US FDA first approval
26 January 1953
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
Capsule
Identifiers
UNII 0TTZ664R7ZRxCUI 8149CAS 59-96-1DrugBank DB00925Q419824

Clinical information

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

Uses

INDICATION AND USAGE Phenoxybenzamine hydrochloride capsules are indicated in the treatment of pheochromocytoma, to control episodes of hypertension and sweating. If tachycardia is excessive, it may be necessary to use a beta -blocking agent concomitantly.

Source: US FDA prescribing information

Dosing overview

The dosage should be adjusted to fit the needs of each patient. Small initial doses should be slowly increased until the desired effect is obtained or the side effects from blockade become troublesome. After each increase, the patient should be observed on that level before instituting another increase. The dosage should be carried to a point where symptomatic relief and/or objective improvement are obtained, but not so high that the side effects from blockade become troublesome. Initially, 10 mg of phenoxybenzamine hydrochloride twice a day. Dosage should be increased every other day, usually to 20 mg to 40 mg 2 or 3 times a day, until an optimal dosage is obtained, as judged by blood pressure control. Long-term use of phenoxybenzamine is not recommended.

Source: US FDA prescribing information

Contraindications

Conditions where a fall in blood pressure may be undesirable, hypersensitivity to the phenoxybenzamine hydrochloride capsules, or any of its components.

Source: US FDA prescribing information

Warnings and precautions

WARNING Phenoxybenzamine hydrochloride-induced alpha -adrenergic blockade leaves beta -adrenergic receptors unopposed. Compounds that stimulate both types of receptors may, therefore, produce an exaggerated hypotensive response and tachycardia.

Source: US FDA prescribing information

Side effects

The following adverse reactions have been observed, but there are insufficient data to support an estimate of their frequency. Autonomic Nervous System*: Postural hypotension, tachycardia, inhibition of ejaculation, nasal congestion, miosis. *These so-called “side effects” are actually evidence of adrenergic blockade and vary according to the degree of blockade. Miscellaneous: Gastrointestinal irritation, drowsiness, fatigue.

Source: US FDA prescribing information

Interactions

2 – Phenoxybenzamine hydrochloride may interact with compounds that stimulate both alpha- and beta- adrenergic receptors (i.e. epinephrine) to produce an exaggerated hypotensive response and tachycardia. Phenoxybenzamine hydrochloride blocks hyperthermia production by levarterenol, and blocks hypothermia production by reserpine.

Source: US FDA prescribing information

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

All presentations

1 presentations of Phenoxybenzamine, sorted by availability.

MedicineManufacturerRegisterAvailability
Phenoxybenzamine 10 mg capsuleOralGeneric name—US FDAAvailable on request

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 26 January 1953Drugs@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 Phenoxybenzamine in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Phenoxybenzamine available for export from India?

Yes, on request. MedsAcross lists 1 presentations of Phenoxybenzamine and sources them for licensed hospitals, importers and physicians against valid import documents.

Is Phenoxybenzamine approved by the US FDA?

Yes. The US FDA first approved Phenoxybenzamine on 26 January 1953, according to Drugs@FDA.

Does Phenoxybenzamine need cold chain shipping?

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

Which ATC class is Phenoxybenzamine in?

Phenoxybenzamine is classified under ATC code C04AX02 (Phenoxybenzamine).

References

  1. Phenoxybenzamine hydrochloride prescribing information (Amneal Pharmaceuticals NY). U.S. National Library of Medicine, DailyMed. Retrieved 3 July 2026

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