Digoxin
- Product NDC
- 68084-680
- 11-digit product format
- 680840680
- Labeler code
- 68084
- Product ID
- 68084-680_9a11370e-d97c-4ade-e053-2995a90a8720
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DIGOXIN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA078556
- Marketing category
- ANDA
- Marketing start
- 2014-09-05
- Marketing end
- 2020-10-31
- Substance
- DIGOXIN
- Active strength
- 250 ug/1
- Pharmacologic classes
- Cardiac Glycoside [EPC],Cardiac Glycosides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record