Doxazosin
- Product NDC
- 68071-5153
- 11-digit product format
- 680715153
- Labeler code
- 68071
- Product ID
- 68071-5153_bbf5ba02-2556-6671-e053-2995a90a8c3b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxazosin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA202824
- Marketing category
- ANDA
- Marketing start
- 2017-06-14
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-5153-1 | 68071515301 | 100 TABLET in 1 BOTTLE (68071-5153-1) | 100 tablet | 2020-01-17 | 0000-00-00 | No | No | Current |