Prazosin Hydrochloride
- Product NDC
- 66993-431
- 11-digit product format
- 669930431
- Labeler code
- 66993
- Product ID
- 66993-431_a6331a1e-125b-43f0-949c-2d8979495b9c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prazosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Prasco Laboratories
- Application
- NDA017442
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2021-08-25
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Prazosin Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PRAZOSIN HYDROCHLORIDE | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | X0Z7454B90 |
| Rxcui | 198141, 312593, 312594 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 66993-431-85 | Prazosin Hydrochloride | 90 in 1 BOTTLE | CAPSULE | 90 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66993-431 | PRAZOSIN HYDROCHLORIDE CAPSULE [PRASCO LABORATORIES] | 5 | Current NDC, Legacy NDC, 1 package rows | 20250215_cbe89216-7dea-43d7-b12e-44ccfb69af3d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66993-431-85 | 66993043185 | 90 CAPSULE in 1 BOTTLE (66993-431-85) | 90 capsule | 2021-08-25 | 0000-00-00 | No | No | Current |