Cardura
- Product NDC
- 0049-2410
- 11-digit product format
- 000492410
- Labeler code
- 0049
- Product ID
- 0049-2410_aded71a7-bfc7-4006-8378-578776e7bfd3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- doxazosin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Roerig
- Application
- NDA019668
- Marketing category
- NDA
- Marketing start
- 2021-10-19
- Marketing end
- 0000-00-00
- Substance
- DOXAZOSIN MESYLATE
- 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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0049-2410-10 | Cardura | 100 in 1 BOTTLE | TABLET | 100 | | 25 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0049-2410 | CARDURA (DOXAZOSIN MESYLATE) TABLET CARDURA (DOXAZOSIN) TABLET [ROERIG] | 24 | Legacy NDC, 1 package rows | 20250425_eefc47bc-c10f-49bb-8ef7-5999f798ab39.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 |
|---|
| 0049-2410-10 | 00049241010 | 100 TABLET in 1 BOTTLE (0049-2410-10) | 100 tablet | 2021-10-19 | 0000-00-00 | No | No | Current |