Prazosin Hydrochloride
- Product NDC
- 50090-2845
- 11-digit product format
- 500902845
- Labeler code
- 50090
- Product ID
- 50090-2845_f8d20ca5-c6bc-4f84-b957-5b16cf7ddddb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prazosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA072575
- Marketing category
- ANDA
- Marketing start
- 1989-02-28
- 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 |
|---|
| 50090-2845-0 | Prazosin Hydrochloride | 1 in 1 BLISTER PACK | CAPSULE | 1 | | 9 |
| 50090-2845-0 | Prazosin Hydrochloride | 32 in 1 BOX, UNIT-DOSE | CAPSULE | 32 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2845 | PRAZOSIN HYDROCHLORIDE CAPSULE [A-S MEDICATION SOLUTIONS] | 9 | Legacy NDC, 2 package rows | 20220609_55e74841-23f1-4cfb-97b2-8bd2d2329b0e.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 |
|---|
| 50090-2845-0 | 50090284500 | 32 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-2845-0) > 1 CAPSULE in 1 BLISTER PACK | 32 blister pack | 2017-02-08 | 0000-00-00 | No | No | Current |