Digoxin
- Product NDC
- 50268-238
- 11-digit product format
- 502680238
- Labeler code
- 50268
- Product ID
- 50268-238_1cfd158a-1cec-9e3d-e063-6394a90afe49
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA214982
- Marketing category
- ANDA
- Marketing start
- 2024-07-11
- Substance
- DIGOXIN
- Active strength
- .125 mg/1
- Pharmacologic classes
- Cardiac Glycoside [EPC], Cardiac Glycosides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Digoxin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIGOXIN | .125 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 73K4184T59 |
| Rxcui | 197604 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50268-238-11 | Digoxin | 1 in 1 BLISTER PACK | TABLET | 1 | | 1 |
| 50268-238-15 | Digoxin | 50 in 1 BOX | TABLET | 50 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50268-238 | DIGOXIN TABLET [AVPAK] | 1 | Current NDC, 2 package rows | 20240712_1cfd4e43-56f0-d182-e063-6394a90ad231.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50268-238-11 | 50268023811 | 1 in 1 BLISTER PACK | | | | | Historical |
| 50268-238-15 | 50268023815 | 50 BLISTER PACK in 1 BOX (50268-238-15) / 1 TABLET in 1 BLISTER PACK (50268-238-11) | 50 blister pack | 2024-07-11 | No | No | Current |