Doxazosin
- Product NDC
- 71335-2803
- 11-digit product format
- 713352803
- Labeler code
- 71335
- Product ID
- 71335-2803_f922ceda-90c9-4aff-8d15-1707a26295d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxazosin Mesylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075536
- Marketing category
- ANDA
- Marketing start
- 2014-08-06
- Substance
- DOXAZOSIN MESYLATE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 86P6PQK0MU | DOXAZOSIN MESYLATE | 77883-43-3 | DOXAZOSIN MESYLATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2803-1 | 71335280301 | 30 TABLET in 1 BOTTLE (71335-2803-1) | 30 tablet | 2025-10-13 | No | No | Historical |
| 71335-2803-2 | 71335280302 | 90 TABLET in 1 BOTTLE (71335-2803-2) | 90 tablet | 2025-10-13 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Doxazosin | Bryant Ranch Prepack | 2025-10-13 | HUMAN PRESCRIPTION DRUG LABEL | 1 |