Doxazosin Mesylate
- Product NDC
- 70518-0184
- 11-digit product format
- 705180184
- Labeler code
- 70518
- Product ID
- 70518-0184_82c433f9-d6a6-2782-e053-2991aa0a6511
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxazosin Mesylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076161
- Marketing category
- ANDA
- Marketing start
- 2017-01-27
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record