DIGOXIN
- Product NDC
- 68071-3011
- 11-digit product format
- 680713011
- Labeler code
- 68071
- Product ID
- 68071-3011_bb12a06b-0078-3cef-e053-2995a90a1ca1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DIGOXIN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- NDA020405
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2014-01-14
- Marketing end
- 0000-00-00
- Substance
- DIGOXIN
- Active strength
- 0 mg/1
- Pharmacologic classes
- Cardiac Glycoside [EPC],Cardiac Glycosides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68071-3011-3 | 68071301103 | 30 TABLET in 1 BOTTLE (68071-3011-3) | 30 tablet | 2017-03-16 | 0000-00-00 | No | No | Current |
| 68071-3011-6 | 68071301106 | 60 TABLET in 1 BOTTLE (68071-3011-6) | 60 tablet | 2017-03-16 | 0000-00-00 | No | No | Current |
| 68071-3011-7 | 68071301107 | 7 TABLET in 1 BOTTLE (68071-3011-7) | 7 tablet | 2017-03-16 | 0000-00-00 | No | No | Current |
| 68071-3011-9 | 68071301109 | 90 TABLET in 1 BOTTLE (68071-3011-9) | 90 tablet | 2017-03-16 | 0000-00-00 | No | No | Current |