Prazosin Hydrochloride
- Product NDC
- 71205-585
- 11-digit product format
- 712050585
- Labeler code
- 71205
- Product ID
- 71205-585_0a2cc210-ad5e-426f-9ddb-25ab2634820f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA071745
- Marketing category
- ANDA
- Marketing start
- 2007-01-18
- 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 |
|---|
| 71205-585-30 | 71205058530 | 30 CAPSULE in 1 BOTTLE (71205-585-30) | 30 capsule | 2021-07-08 | No | No | Historical |
| 71205-585-60 | 71205058560 | 60 CAPSULE in 1 BOTTLE (71205-585-60) | 60 capsule | 2021-07-08 | No | No | Historical |
| 71205-585-90 | 71205058590 | 90 CAPSULE in 1 BOTTLE (71205-585-90) | 90 capsule | 2021-07-08 | No | No | Historical |