Digoxin
- Product NDC
- 50090-4449
- 11-digit product format
- 500904449
- Labeler code
- 50090
- Product ID
- 50090-4449_8b075237-a1c9-4976-a068-5ab798ed7bbc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077002
- Marketing category
- ANDA
- Marketing start
- 2007-10-30
- Marketing end
- 0000-00-00
- Substance
- DIGOXIN
- Active strength
- 250 ug/1
- Pharmacologic classes
- Cardiac Glycoside [EPC],Cardiac Glycosides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 50090-4449-1 | 50090444901 | 100 TABLET in 1 BOTTLE, PLASTIC (50090-4449-1) | 100 tablet | 2019-08-05 | 0000-00-00 | No | No | Current |