Digoxin
- Product NDC
- 71335-0282
- 11-digit product format
- 713350282
- Labeler code
- 71335
- Product ID
- 71335-0282_7fecc5ac-fa18-4aad-a3f9-89e58e0b997e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076268
- Marketing category
- ANDA
- Marketing start
- 2002-07-26
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71335-0282-1 | EA - Each | 71335-0282 | 7b61b349-c7ee-4586-a515-c235928c5794 | 1 | 2018-01-12 |
| 71335-0282-2 | EA - Each | 71335-0282 | 1b33658e-7d2d-4427-b74d-e4ac243703b4 | 1 | 2018-01-12 |
| 71335-0282-3 | EA - Each | 71335-0282 | 2a9c1e60-05a1-4e07-afa7-f71383fe4b63 | 1 | 2018-01-12 |
| 71335-0282-4 | EA - Each | 71335-0282 | 15595d28-a194-44e0-aab6-876d45b1be02 | 1 | 2018-01-12 |
| 71335-0282-5 | EA - Each | 71335-0282 | 3d6c3e4e-3607-40b0-962d-71f459a7f0f7 | 1 | 2018-01-12 |
| 71335-0282-6 | EA - Each | 71335-0282 | 5b681138-e2a8-4745-b249-5dc3229e6e31 | 1 | 2018-01-12 |