Doxazosin Mesylate
- Product NDC
- 53808-1107
- 11-digit product format
- 538081107
- Labeler code
- 53808
- Product ID
- 53808-1107_66e847f5-91de-4ec1-8b28-96ce2f036326
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxazosin Mesylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DOH CENTRAL PHARMACY
- Application
- ANDA076161
- Marketing category
- ANDA
- Marketing start
- 2017-12-14
- 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
- 2020-12-31
- 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 |
|---|
| 53808-1107-1 | Doxazosin Mesylate | 30 in 1 BLISTER PACK | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53808-1107 | DOXAZOSIN MESYLATE TABLET [DOH CENTRAL PHARMACY] | 1 | Legacy NDC, 1 package rows | 20190116_80dbf08b-e522-43ca-9575-5db446528252.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 |
|---|
| 53808-1107-1 | 53808110701 | 30 TABLET in 1 BLISTER PACK (53808-1107-1) | 30 tablet | 2017-12-14 | 0000-00-00 | No | No | Current |