Doxazosin
- Product NDC
- 68645-465
- 11-digit product format
- 686450465
- Labeler code
- 68645
- Product ID
- 68645-465_814ec517-9a88-4263-9c8b-c51188503fdb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxazosin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Legacy Pharmaceutical Packaging, LLC
- Application
- ANDA075580
- Marketing category
- ANDA
- Marketing start
- 2011-07-14
- Marketing end
- 2020-06-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record