Prazosin Hydrochloride
- Product NDC
- 71335-1724
- 11-digit product format
- 713351724
- Labeler code
- 71335
- Product ID
- 71335-1724_d2abd3fa-0134-4000-b9a5-ac5266c76d7d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prazosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA072575
- Marketing category
- ANDA
- Marketing start
- 1989-02-28
- Substance
- PRAZOSIN HYDROCHLORIDE
- Active strength
- 1 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
Additional Listing Data
- Finished product
- Yes
- Brand name base
- Prazosin Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients
| Ingredient | Strength |
|---|
| PRAZOSIN HYDROCHLORIDE | 1 mg/1 |
Harmonized Identifiers
| Field | Values |
|---|
| Unii | X0Z7454B90 |
| Rxcui | 312593 |
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1724-1 | 71335172401 | 30 CAPSULE in 1 BOTTLE (71335-1724-1) | 30 capsule | 2020-11-25 | 0000-00-00 | No | No | Current |
| 71335-1724-2 | 71335172402 | 100 CAPSULE in 1 BOTTLE (71335-1724-2) | 100 capsule | 2022-07-01 | 0000-00-00 | No | No | Current |
| 71335-1724-3 | 71335172403 | 60 CAPSULE in 1 BOTTLE (71335-1724-3) | 60 capsule | 2021-01-12 | 0000-00-00 | No | No | Current |
| 71335-1724-4 | 71335172404 | 28 CAPSULE in 1 BOTTLE (71335-1724-4) | 28 capsule | 2022-07-01 | 0000-00-00 | No | No | Current |
| 71335-1724-5 | 71335172405 | 90 CAPSULE in 1 BOTTLE (71335-1724-5) | 90 capsule | 2022-07-01 | 0000-00-00 | No | No | Current |