Digoxin
- Product NDC
- 58118-1240
- 11-digit product format
- 581181240
- Labeler code
- 58118
- Product ID
- 58118-1240_8d6e5457-7016-350c-e053-2995a90a88e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, LLC
- Application
- ANDA077002
- Marketing category
- ANDA
- Marketing start
- 2007-10-30
- Marketing end
- 0000-00-00
- Substance
- DIGOXIN
- Active strength
- 125 ug/1
- Pharmacologic classes
- Cardiac Glycoside [EPC],Cardiac Glycosides [CS]
- 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 |
|---|
| 58118-1240-8 | Digoxin | 30 in 1 BLISTER PACK | TABLET | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58118-1240 | DIGOXIN TABLET [CLINICAL SOLUTIONS WHOLESALE, LLC] | 3 | Legacy NDC, 1 package rows | 20190712_00d8b2a1-064b-4b33-a1ca-cbf1b0aa294f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 58118-1240-8 | 58118124008 | 30 in 1 BLISTER PACK | Historical |