Digoxin
- Product NDC
- 50090-5276
- 11-digit product format
- 500905276
- Labeler code
- 50090
- Product ID
- 50090-5276_3c5b356c-ec49-44fb-a34c-9c68d7edfafa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076268
- Marketing category
- ANDA
- Marketing start
- 2019-04-01
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 73K4184T59 | DIGOXIN | 20830-75-5 | DIGOXIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5276-1 | 50090527601 | 100 TABLET in 1 BOTTLE (50090-5276-1) | 100 tablet | 2020-10-21 | 0000-00-00 | No | No | Current |