Doxazosin
- Product NDC
- 66267-378
- 11-digit product format
- 662670378
- Labeler code
- 66267
- Product ID
- 66267-378_9cbea39d-4d77-90a8-e053-2a95a90a580c
- 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
- 8 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