prazosin hydrochloride
- Product NDC
- 67046-1532
- 11-digit product format
- 670461532
- Labeler code
- 67046
- Product ID
- 67046-1532_30b703e8-8816-bd6e-e063-6294a90a2610
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prazosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Coupler, LLC
- Application
- ANDA215697
- Marketing category
- ANDA
- Marketing start
- 2025-03-19
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- prazosin hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PRAZOSIN HYDROCHLORIDE | 2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | X0Z7454B90 |
| Rxcui | 312594 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67046-1532-3 | prazosin hydrochloride | 30 in 1 BLISTER PACK | CAPSULE | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-1532 | PRAZOSIN HYDROCHLORIDE CAPSULE [COUPLER, LLC] | 1 | Current NDC, 1 package rows | 20250322_30b70064-79e1-b8a9-e063-6394a90a69cb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67046-1532-3 | 67046153203 | 30 CAPSULE in 1 BLISTER PACK (67046-1532-3) | 30 capsule | 2025-03-19 | No | No | Historical |