Digoxin
- Product NDC
- 68071-4469
- 11-digit product format
- 680714469
- Labeler code
- 68071
- Product ID
- 68071-4469_6e8cd19e-59fd-d0fa-e053-2a91aa0a04c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077002
- Marketing category
- ANDA
- Marketing start
- 2007-10-30
- 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