Doxazosin
- Product NDC
- 82804-087
- 11-digit product format
- 828040087
- Labeler code
- 82804
- Product ID
- 82804-087_1d8ff659-8129-4dca-9e8f-13b97240d1e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxazosin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA075580
- Marketing category
- ANDA
- Marketing start
- 2011-07-14
- Substance
- DOXAZOSIN MESYLATE
- Active strength
- 4 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 |
| NW1291F1W8 | DOXAZOSIN | 74191-85-8 | Doxazosin |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-087-30 | 82804008730 | 30 TABLET in 1 BOTTLE (82804-087-30) | 30 tablet | 2024-06-20 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Doxazosin | Proficient Rx LP | 2024-06-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |