Digoxin
- Product NDC
- 71335-1540
- 11-digit product format
- 713351540
- Labeler code
- 71335
- Product ID
- 71335-1540_fdede3df-ff69-4488-9812-33c00df531de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076268
- Marketing category
- ANDA
- Marketing start
- 2019-04-01
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 73K4184T59 | DIGOXIN | 20830-75-5 | DIGOXIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1540-1 | 71335154001 | 30 TABLET in 1 BOTTLE (71335-1540-1) | 30 tablet | 2020-03-24 | 0000-00-00 | No | No | Current |
| 71335-1540-2 | 71335154002 | 90 TABLET in 1 BOTTLE (71335-1540-2) | 90 tablet | 2020-03-24 | 0000-00-00 | No | No | Current |
| 71335-1540-3 | 71335154003 | 15 TABLET in 1 BOTTLE (71335-1540-3) | 15 tablet | 2020-03-24 | 0000-00-00 | No | No | Current |
| 71335-1540-4 | 71335154004 | 6 TABLET in 1 BOTTLE (71335-1540-4) | 6 tablet | 2020-03-24 | 0000-00-00 | No | No | Current |
| 71335-1540-5 | 71335154005 | 60 TABLET in 1 BOTTLE (71335-1540-5) | 60 tablet | 2020-03-24 | 0000-00-00 | No | No | Current |
| 71335-1540-6 | 71335154006 | 100 TABLET in 1 BOTTLE (71335-1540-6) | 100 tablet | 2020-03-24 | 0000-00-00 | No | No | Current |