Digoxin
- Product NDC
- 50090-4432
- 11-digit product format
- 500904432
- Labeler code
- 50090
- Product ID
- 50090-4432_ce02701a-e32f-4d1b-b99b-79e293e180ab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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 |
|---|
| 50090-4432-1 | Digoxin | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4432 | DIGOXIN TABLET [A-S MEDICATION SOLUTIONS] | 2 | Legacy NDC, 1 package rows | 20190726_bdc24f5d-6c62-4474-b551-ac2ff907a24c.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 |
|---|
| 50090-4432-1 | 50090443201 | 100 TABLET in 1 BOTTLE, PLASTIC (50090-4432-1) | 100 tablet | 2019-07-19 | 0000-00-00 | No | No | Current |