Prazosin Hydrochloride
- Product NDC
- 63629-8756
- 11-digit product format
- 636298756
- Labeler code
- 63629
- Product ID
- 63629-8756_31764d63-40c5-46f3-908f-c6d917cb8005
- 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 |
|---|
| 63629-8756-1 | 63629875601 | 100 CAPSULE in 1 BOTTLE (63629-8756-1) | 100 capsule | 2021-08-20 | No | No | Historical |