Prazosin HCL
- Product NDC
- 72189-436
- 11-digit product format
- 721890436
- Labeler code
- 72189
- Product ID
- 72189-436_22053934-8b9c-cece-e063-6394a90a86a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin HCL
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA215697
- Marketing category
- ANDA
- Marketing start
- 2023-03-13
- 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 HCL
- 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 |
|---|
| 72189-436-30 | Prazosin HCL | 30 in 1 BOTTLE | CAPSULE | 30 | | 4 |
| 72189-436-60 | Prazosin HCL | 60 in 1 BOTTLE | CAPSULE | 60 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-436 | PRAZOSIN HCL CAPSULE [DIRECT_RX] | 4 | Current NDC, 2 package rows | 20240915_f6c9eef9-c016-9020-e053-6294a90a1cd8.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 |
|---|
| 72189-436-30 | 72189043630 | 30 CAPSULE in 1 BOTTLE (72189-436-30) | 30 capsule | 2023-03-13 | No | No | Current |
| 72189-436-60 | 72189043660 | 60 CAPSULE in 1 BOTTLE (72189-436-60) | 60 capsule | 2023-03-13 | No | No | Current |