United States · FDA National Drug Code directory

PHENOXYBENZAMINE HYDROCHLORIDE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
35573-473_609aa41e-4cb5-4cdf-9137-f429c21b4fab
Product NDC
35573-473
Form
CAPSULE
Composition / generic term
PHENOXYBENZAMINE HYDROCHLORIDE
Labeler
Burel Pharmaceuticals, LLC
Marketing category
ANDA
Marketing start / end (source format)
20230508
Source listing expiry
20261231

Source-listed ingredients

  • PHENOXYBENZAMINE HYDROCHLORIDE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE in 1 BOTTLE (35573-473-02) · 35573-473-02

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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PHENOXYBENZAMINE HYDROCHLORIDE — United States | Molindra Medicines