Digoxin
- Product NDC
- 63629-2579
- 11-digit product format
- 636292579
- Labeler code
- 63629
- Product ID
- 63629-2579_248f828b-b8f2-421b-bd56-e715a55514e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077002
- Marketing category
- ANDA
- Marketing start
- 2007-10-30
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2579-1 | 63629257901 | 30 TABLET in 1 BOTTLE (63629-2579-1) | 30 tablet | 2022-02-21 | 0000-00-00 | No | No | Current |
| 63629-2579-2 | 63629257902 | 90 TABLET in 1 BOTTLE (63629-2579-2) | 90 tablet | 2011-06-16 | 0000-00-00 | No | No | Current |
| 63629-2579-3 | 63629257903 | 15 TABLET in 1 BOTTLE (63629-2579-3) | 15 tablet | 2011-10-26 | 0000-00-00 | No | No | Current |
| 63629-2579-4 | 63629257904 | 6 TABLET in 1 BOTTLE (63629-2579-4) | 6 tablet | 2022-02-21 | 0000-00-00 | No | No | Current |
| 63629-2579-5 | 63629257905 | 60 TABLET in 1 BOTTLE (63629-2579-5) | 60 tablet | 2022-02-21 | 0000-00-00 | No | No | Current |
| 63629-2579-6 | 63629257906 | 100 TABLET in 1 BOTTLE (63629-2579-6) | 100 tablet | 2022-02-21 | 0000-00-00 | No | No | Current |
| 63629-2579-7 | 63629257907 | 10 TABLET in 1 BOTTLE (63629-2579-7) | 10 tablet | 2022-02-21 | 0000-00-00 | No | No | Current |