Doxazosin Mesylate
- Product NDC
- 50090-0735
- 11-digit product format
- 500900735
- Labeler code
- 50090
- Product ID
- 50090-0735_40aad14a-5dc4-4602-8f7a-58dfd47b4004
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxazosin Mesylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076161
- Marketing category
- ANDA
- Marketing start
- 2004-06-10
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record