Prazosin Hydrochloride
- Product NDC
- 63629-8750
- 11-digit product format
- 636298750
- Labeler code
- 63629
- Product ID
- 63629-8750_5780feee-f1ad-4426-b29c-80cc0a03c639
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071745
- Marketing category
- ANDA
- Marketing start
- 2007-02-22
- 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
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 |
|---|
| 63629-8750-1 | 63629875001 | 1000 CAPSULE in 1 BOTTLE (63629-8750-1) | 1000 capsule | 2021-08-20 | No | No | Historical |