Prazosin Hydrochloride
- Product NDC
- 50090-0379
- 11-digit product format
- 500900379
- Labeler code
- 50090
- Product ID
- 50090-0379_7e538bcb-8e17-499e-b599-f5d17d48abc3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA071745
- Marketing category
- ANDA
- Marketing start
- 2007-02-22
- Marketing end
- 0000-00-00
- Substance
- PRAZOSIN HYDROCHLORIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- alpha-Adrenergic Blocker [EPC],Adrenergic alpha-Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-0379-1 | Prazosin Hydrochloride | 30 in 1 BOTTLE | CAPSULE | 30 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0379 | PRAZOSIN HYDROCHLORIDE CAPSULE [A-S MEDICATION SOLUTIONS] | 10 | Legacy NDC, 1 package rows | 20210219_2c7cd673-c8f2-4d22-b48c-49e616409c56.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 |
|---|
| 50090-0379-1 | 50090037901 | 30 CAPSULE in 1 BOTTLE (50090-0379-1) | 30 capsule | 2016-06-29 | 0000-00-00 | No | No | Current |