Prazosin Hydrochloride
- Product NDC
- 50090-5697
- 11-digit product format
- 500905697
- Labeler code
- 50090
- Product ID
- 50090-5697_d8a790c5-2a7d-4801-b6cf-3d2b454b83de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA210971
- Marketing category
- ANDA
- Marketing start
- 2018-10-03
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-5697-0 | Prazosin Hydrochloride | 32 in 1 CARTON | CAPSULE | 32 | | 1 |
| 50090-5697-0 | Prazosin Hydrochloride | 1 in 1 BLISTER PACK | CAPSULE | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5697 | PRAZOSIN HYDROCHLORIDE CAPSULE [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 2 package rows | 20221229_b8e957e8-816c-4fcb-ba35-f20b9421ae59.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 |
|---|
| 50090-5697-0 | 50090569700 | 32 BLISTER PACK in 1 CARTON (50090-5697-0) > 1 CAPSULE in 1 BLISTER PACK | 32 blister pack | 2021-09-22 | 0000-00-00 | No | No | Current |