prazosin hydrochloride
- Product NDC
- 82804-089
- 11-digit product format
- 828040089
- Labeler code
- 82804
- Product ID
- 82804-089_2a928735-179f-4637-8c4e-3b5e01d45bf2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prazosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA215697
- Marketing category
- ANDA
- Marketing start
- 2023-01-03
- Substance
- PRAZOSIN HYDROCHLORIDE
- Active strength
- 5 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 | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | X0Z7454B90 |
| Rxcui | 198141 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82804-089-90 | prazosin hydrochloride | 90 in 1 BOTTLE | CAPSULE | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82804-089 | PRAZOSIN HYDROCHLORIDE CAPSULE [PROFICIENT RX LP] | 1 | Current NDC, 1 package rows | 20240316_2a928735-179f-4637-8c4e-3b5e01d45bf2.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 |
|---|
| 82804-089-90 | 82804008990 | 90 CAPSULE in 1 BOTTLE (82804-089-90) | 90 capsule | 2024-03-14 | No | No | Current |