Prazosin HCL
- Product NDC
- 72189-540
- 11-digit product format
- 721890540
- Labeler code
- 72189
- Product ID
- 72189-540_13018fa7-5e31-ed92-e063-6394a90a4427
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin HCL
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA215697
- Marketing category
- ANDA
- Marketing start
- 2024-03-06
- Substance
- PRAZOSIN HYDROCHLORIDE
- Active strength
- 2 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 |
|---|
| 72189-540-30 | 72189054030 | 30 CAPSULE in 1 BOTTLE (72189-540-30) | 30 capsule | 2024-03-06 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Prazosin HCL | Direct_Rx | 2024-03-06 | HUMAN PRESCRIPTION DRUG LABEL | 1 |