DIGOXIN
- Product NDC
- 66267-078
- 11-digit product format
- 662670078
- Labeler code
- 66267
- Product ID
- 66267-078_9cbd45e2-18ee-16e3-e053-2a95a90a556d
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66267-078-30 | 66267007830 | 30 TABLET in 1 BOTTLE (66267-078-30) | 30 tablet | 2016-09-30 | 0000-00-00 | No | No | Current |