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
71335-9672_8b34ead9-50b9-4731-8a62-616b15c55401
Product NDC
71335-9672
Form
TABLET
Composition / generic term
Doxazosin Mesylate
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20180417 / 20270831

Source-listed ingredients

  • DOXAZOSIN MESYLATE — 4 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (71335-9672-1) · 71335-9672-1
  • 30 TABLET in 1 BOTTLE (71335-9672-2) · 71335-9672-2
  • 60 TABLET in 1 BOTTLE (71335-9672-3) · 71335-9672-3
  • 90 TABLET in 1 BOTTLE (71335-9672-4) · 71335-9672-4

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.

Browse United States records →