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
- 68084-851_3f045cb5-3d97-806a-e063-6294a90aa301
- Product NDC
- 68084-851
- Form
- TABLET
- Composition / generic term
- Doxazosin
- Labeler
- American Health Packaging
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140916
- Source listing expiry
- 20261231
Source-listed ingredients
- DOXAZOSIN MESYLATE — 2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-851-01) / 1 TABLET in 1 BLISTER PACK (68084-851-11) · 68084-851-01
- 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-851-25) / 1 TABLET in 1 BLISTER PACK (68084-851-95) · 68084-851-25
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 →