Digoxin
- Product NDC
- 52584-410
- 11-digit product format
- 525840410
- Labeler code
- 52584
- Product ID
- 52584-410_39654037-4e1f-4e3a-96b2-fc71adedcecf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc
- Application
- ANDA083391
- Marketing category
- ANDA
- Marketing start
- 2010-07-01
- Marketing end
- 2024-11-30
- Substance
- DIGOXIN
- Active strength
- 0 mg/mL
- 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 |
|---|
| 52584-410-31 | 52584041031 | 1 AMPULE in 1 BAG (52584-410-31) > 2 mL in 1 AMPULE | 1 ampule | 2010-07-01 | 2024-11-30 | No | No | Current |