LANOXIN
- Product NDC
- 65084-455
- 11-digit product format
- 650840455
- Labeler code
- 65084
- Product ID
- 65084-455_509fb279-dc81-4029-8383-16acc9afcdc9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mckesson Rxpak Inc
- Application
- NDA020405
- Marketing category
- NDA
- Marketing start
- 2012-09-30
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record