Finished product reference
Phenoxybenzamine
Capsule · Oral · 10 mg
- List code
- 984
Indications
INDICATIONS AND USAGE Phenoxybenzamine Hydrochloride Capsule, USP is 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.
Dosage and administration (summary)
DOSAGE AND ADMINISTRATION 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.
Contraindications
CONTRAINDICATIONS Conditions where a fall in blood pressure may be undesirable; hypersensitivity to the drug or any of its components.
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.
Pregnancy
Pregnancy Teratogenic Effects Adequate reproductive studies in animals have not been performed with phenoxybenzamine hydrochloride. It is also not known whether phenoxybenzamine hydrochloride can cause fetal harm when administered to a pregnant woman.
Storage and supply
HOW SUPPLIED Phenoxybenzamine Hydrochloride Capsules USP, 10 mg: are supplied as transparent red/transparent red size 3 hard gelatin capsule shells, imprinted with ‘C118’ on cap and ‘10’ on body with white ink, filled with white to off white powder, in bottles of 100 (NDC 16571-874-01)
Source: Phenoxybenzamine Hydrochloride (Phenoxybenzamine Hydrochloride) — US FDA prescribing information, 2026-06-18, DailyMed. Summarised and shortened; the full label governs. Iranian registration, indications and labelling may differ.
Reference information for professional sourcing and registration enquiries, not medical advice or a promotion. Drug information is condensed from US FDA prescribing information (public domain, via openFDA and DailyMed) and does not replace the product’s approved labelling in Iran. Availability, origin and documentation are confirmed per enquiry.
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