Doxazosin
- Product NDC
- 50090-0704
- 11-digit product format
- 500900704
- Labeler code
- 50090
- Product ID
- 50090-0704_33c2d704-0230-4323-af6a-01c55e6616ed
- 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
- 2 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]
- 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 |
|---|
| 50090-0704-0 | Doxazosin | 30 in 1 BOTTLE | TABLET | 30 | | 30 |
| 50090-0704-1 | Doxazosin | 100 in 1 BOTTLE | TABLET | 100 | | 30 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0704 | DOXAZOSIN TABLET [A-S MEDICATION SOLUTIONS] | 28 | Legacy NDC, 2 package rows | 20240615_bfea0b5b-9354-490f-88ff-008134077d24.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 |
|---|
| 50090-0704-0 | 50090070400 | 30 TABLET in 1 BOTTLE (50090-0704-0) | 30 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0704-1 | 50090070401 | 100 TABLET in 1 BOTTLE (50090-0704-1) | 100 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |