prazosin hydrochloride
- Product NDC
- 82804-089
- 11-digit product format
- 828040089
- Labeler code
- 82804
- Product ID
- 82804-089_2a928735-179f-4637-8c4e-3b5e01d45bf2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prazosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA215697
- Marketing category
- ANDA
- Marketing start
- 2023-01-03
- Substance
- PRAZOSIN HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| X0Z7454B90 | PRAZOSIN HYDROCHLORIDE | 19237-84-4 | PRAZOSIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-089-90 | 82804008990 | 90 CAPSULE in 1 BOTTLE (82804-089-90) | 90 capsule | 2024-03-14 | No | No | Historical |