Doxazosin
- Product NDC
- 50090-2434
- 11-digit product format
- 500902434
- Labeler code
- 50090
- Product ID
- 50090-2434_62aca8a1-3d26-4827-a585-7be7d38f5623
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxazosin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075580
- Marketing category
- ANDA
- Marketing start
- 2011-07-14
- Marketing end
- 0000-00-00
- Substance
- DOXAZOSIN MESYLATE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 50090-2434-1 | Doxazosin | 100 in 1 BOTTLE | TABLET | 100 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2434 | DOXAZOSIN TABLET [A-S MEDICATION SOLUTIONS] | 10 | Legacy NDC, 1 package rows | 20181211_40620f8e-fd36-4634-9cf6-120138d23187.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-2434-1 | 50090243401 | 100 in 1 BOTTLE | Historical |