Prazosin
- Product NDC
- 0527-4182
- 11-digit product format
- 005274182
- Labeler code
- 0527
- Product ID
- 0527-4182_41beba09-90c1-42cc-bfba-ac8a84d09649
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA214083
- Marketing category
- ANDA
- Marketing start
- 2024-01-03
- 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
- 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, 312593, 312594 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0527-4182-37 | Prazosin | 100 in 1 BOTTLE | CAPSULE | 100 | | 8 |
| 0527-4182-42 | Prazosin | 250 in 1 BOTTLE | CAPSULE | 250 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0527-4182 | PRAZOSIN CAPSULE [LANNETT COMPANY, INC.] | 8 | Current NDC, 2 package rows | 20250316_94021822-60cb-4da6-b809-f565e1d6452d.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 |
|---|
| 0527-4182-37 | 00527418237 | 100 CAPSULE in 1 BOTTLE (0527-4182-37) | 100 capsule | 2024-01-03 | No | No | Current |
| 0527-4182-42 | 00527418242 | 250 CAPSULE in 1 BOTTLE (0527-4182-42) | 250 capsule | 2024-01-03 | No | No | Current |