Doxazosin
- Product NDC
- 68788-7328
- 11-digit product format
- 687887328
- Labeler code
- 68788
- Product ID
- 68788-7328_2887b59c-a676-48ce-99ab-a712d54a5da8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxazosin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA202824
- Marketing category
- ANDA
- Marketing start
- 2019-03-12
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7328-3 | 68788732803 | 30 TABLET in 1 BOTTLE (68788-7328-3) | 30 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |
| 68788-7328-6 | 68788732806 | 60 TABLET in 1 BOTTLE (68788-7328-6) | 60 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |
| 68788-7328-9 | 68788732809 | 90 TABLET in 1 BOTTLE (68788-7328-9) | 90 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |