Prazosin Hydrochloride
- Product NDC
- 63629-8750
- 11-digit product format
- 636298750
- Labeler code
- 63629
- Product ID
- 63629-8750_5780feee-f1ad-4426-b29c-80cc0a03c639
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA071745
- Marketing category
- ANDA
- Marketing start
- 2007-02-22
- 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
- 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 | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | X0Z7454B90 |
| Rxcui | 312593 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-8750-1 | Prazosin Hydrochloride | 1000 in 1 BOTTLE | CAPSULE | 1000 | | 102 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-8750 | PRAZOSIN HYDROCHLORIDE CAPSULE [BRYANT RANCH PREPACK] | 102 | Current NDC, Legacy NDC, 1 package rows | 20240112_ce926a30-d417-4fc1-8aa3-71405f09ec5e.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 |
|---|
| 63629-8750-1 | 63629875001 | 1000 CAPSULE in 1 BOTTLE (63629-8750-1) | 1000 capsule | 2021-08-20 | 0000-00-00 | No | No | Current |