Digoxin
- Product NDC
- 82804-244
- 11-digit product format
- 828040244
- Labeler code
- 82804
- Product ID
- 82804-244_42d079a7-def1-4220-b71f-db2651966ffe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA076268
- Marketing category
- ANDA
- Marketing start
- 2022-09-01
- Substance
- DIGOXIN
- Active strength
- 250 ug/1
- Pharmacologic classes
- Cardiac Glycoside [EPC], Cardiac Glycosides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 73K4184T59 | DIGOXIN | 20830-75-5 | DIGOXIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-244-90 | 82804024490 | 90 TABLET in 1 BOTTLE (82804-244-90) | 90 tablet | 2025-09-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Digoxin | Proficient Rx LP | 2025-09-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |