Digoxin
- Product NDC
- 51407-126
- 11-digit product format
- 514070126
- Labeler code
- 51407
- Product ID
- 51407-126_79012548-92a1-af5e-e053-2991aa0ae153
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply
- Application
- ANDA076363
- Marketing category
- ANDA
- Marketing start
- 2003-01-31
- 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