Doxazosin
- Product NDC
- 68788-7149
- 11-digit product format
- 687887149
- Labeler code
- 68788
- Product ID
- 68788-7149_c75c470f-7811-4bba-9143-1fde960697f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxazosin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA202824
- Marketing category
- ANDA
- Marketing start
- 2018-04-23
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 68788-7149-3 | 68788714903 | 30 TABLET in 1 BOTTLE (68788-7149-3) | 30 tablet | 2018-04-23 | 0000-00-00 | No | No | Current |
| 68788-7149-6 | 68788714906 | 60 TABLET in 1 BOTTLE (68788-7149-6) | 60 tablet | 2018-04-23 | 0000-00-00 | No | No | Current |
| 68788-7149-9 | 68788714909 | 90 TABLET in 1 BOTTLE (68788-7149-9) | 90 tablet | 2018-04-23 | 0000-00-00 | No | No | Current |