Prazosin Hydrochloride
- Product NDC
- 55289-536
- 11-digit product format
- 552890536
- Labeler code
- 55289
- Product ID
- 55289-536_41acd2b1-05fc-f6ff-e063-6394a90abda4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prazosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA072575
- Marketing category
- ANDA
- Marketing start
- 1989-02-28
- 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 |
|---|
| 55289-536-60 | Prazosin Hydrochloride | 60 in 1 BOTTLE, PLASTIC | CAPSULE | 60 | | 14 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55289-536 | PRAZOSIN HYDROCHLORIDE CAPSULE [PD-RX PHARMACEUTICALS, INC.] | 13 | Current NDC, Legacy NDC, 1 package rows | 20221221_e5e129aa-2ee3-4c12-a327-5d5382cf2310.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 |
|---|
| 55289-536-60 | 55289053660 | 60 CAPSULE in 1 BOTTLE, PLASTIC (55289-536-60) | 60 capsule | 1994-07-22 | 0000-00-00 | No | No | Current |