Digoxin
- Product NDC
- 55154-3375
- 11-digit product format
- 551543375
- Labeler code
- 55154
- Product ID
- 55154-3375_851d7cd2-4a91-4b36-829a-7faa00e02886
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA077002
- Marketing category
- ANDA
- Marketing start
- 2009-06-10
- Marketing end
- 0000-00-00
- Substance
- DIGOXIN
- Active strength
- 250 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