Digoxin
- Product NDC
- 70518-1036
- 11-digit product format
- 705181036
- Labeler code
- 70518
- Product ID
- 70518-1036_e2bf6d67-c5fa-f8db-e053-2a95a90ad83e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077002
- Marketing category
- ANDA
- Marketing start
- 2018-02-28
- 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
- 2023-12-31
- 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 |
|---|
| 70518-1036-0 | 70518103600 | 30 TABLET in 1 BLISTER PACK (70518-1036-0) | 30 tablet | 2018-02-28 | 0000-00-00 | No | No | Current |