Digoxin
- Product NDC
- 0904-6886
- 11-digit product format
- 009046886
- Labeler code
- 0904
- Product ID
- 0904-6886_5b0297ba-497e-46af-b027-6d46d9409384
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA077002
- Marketing category
- ANDA
- Marketing start
- 2009-06-10
- 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