Prazosin Hydrochloride
- Product NDC
- 70518-3375
- 11-digit product format
- 705183375
- Labeler code
- 70518
- Product ID
- 70518-3375_e930de88-39db-100c-e053-2a95a90a713f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA071745
- Marketing category
- ANDA
- Marketing start
- 2022-03-01
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 70518-3375-0 | 70518337500 | 30 CAPSULE in 1 BLISTER PACK (70518-3375-0) | 30 capsule | 2022-03-01 | 0000-00-00 | No | No | Current |