DIGITEK
- Product NDC
- 42292-002
- 11-digit product format
- 422920002
- Labeler code
- 42292
- Product ID
- 42292-002_d3af12b4-8e73-2323-e053-2a95a90ac0e5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA040282
- Marketing category
- ANDA
- Marketing start
- 2015-05-06
- Marketing end
- 2023-02-28
- Substance
- DIGOXIN
- Active strength
- 0 mg/1
- Pharmacologic classes
- Cardiac Glycoside [EPC],Cardiac Glycosides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 42292-002-20 | 42292000220 | 100 BLISTER PACK in 1 CARTON (42292-002-20) > 1 TABLET in 1 BLISTER PACK (42292-002-01) | 100 blister pack | 2015-05-06 | 0000-00-00 | No | No | Current |