prazosin hydrochloride
- Product NDC
- 68071-2972
- 11-digit product format
- 680712972
- Labeler code
- 68071
- Product ID
- 68071-2972_292cb35f-8034-23a8-e063-6294a90aef4c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prazosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA215697
- Marketing category
- ANDA
- Marketing start
- 2023-01-03
- 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 |
|---|
| 68071-2972-1 | 68071297201 | 100 CAPSULE in 1 BOTTLE (68071-2972-1) | 100 capsule | 2023-04-10 | No | No | Historical |