United States · FDA National Drug Code directory

Doxazosin

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
71335-2395_17442115-4aac-79b0-e063-6294a90a84bc
Product NDC
71335-2395
Form
TABLET
Composition / generic term
Doxazosin
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20170831
Source listing expiry
20261231

Source-listed ingredients

  • DOXAZOSIN MESYLATE — 2 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (71335-2395-1) · 71335-2395-1
  • 60 TABLET in 1 BOTTLE (71335-2395-2) · 71335-2395-2
  • 90 TABLET in 1 BOTTLE (71335-2395-3) · 71335-2395-3
  • 28 TABLET in 1 BOTTLE (71335-2395-4) · 71335-2395-4
  • 18 TABLET in 1 BOTTLE (71335-2395-5) · 71335-2395-5

Source and coverage

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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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