Doxazosin
- Product NDC
- 66267-430
- 11-digit product format
- 662670430
- Labeler code
- 66267
- Product ID
- 66267-430_9cade8b8-7bea-f3d8-e053-2995a90a4b92
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxazosin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA202824
- Marketing category
- ANDA
- Marketing start
- 2015-04-22
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record