DOXAZOSIN
- Product NDC
- 72189-117
- 11-digit product format
- 721890117
- Labeler code
- 72189
- Product ID
- 72189-117_2be8ef13-7e70-fc50-e063-6394a90a0f27
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOXAZOSIN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- direct rx
- Application
- ANDA202824
- Marketing category
- ANDA
- Marketing start
- 2020-12-02
- Substance
- DOXAZOSIN MESYLATE
- Active strength
- 2 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 |
|---|
| 72189-117-60 | 72189011760 | 60 TABLET in 1 BOTTLE (72189-117-60) | 60 tablet | 2020-12-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| DOXAZOSIN | direct rx | 2025-01-17 | HUMAN PRESCRIPTION DRUG LABEL | 2 |