Prazosin Hydrochloride
- Product NDC
- 55154-4391
- 11-digit product format
- 551544391
- Labeler code
- 55154
- Product ID
- 55154-4391_63dc1076-1048-412f-b302-91da0553c538
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prazosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA072575
- Marketing category
- ANDA
- Marketing start
- 1998-10-05
- Marketing end
- 0000-00-00
- Substance
- PRAZOSIN HYDROCHLORIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- alpha-Adrenergic Blocker [EPC],Adrenergic alpha-Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record