Digoxin
- Product NDC
- 71335-2464
- 11-digit product format
- 713352464
- Labeler code
- 71335
- Product ID
- 71335-2464_20347bf0-6858-4d38-b1f6-8ec210d2bb1a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Digoxin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIGOXIN | 250 ug/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 73K4184T59 |
| Rxcui | 197606 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2464-1 | Digoxin | 1000 in 1 BOTTLE | TABLET | 1000 | | 100 |
| 71335-2464-2 | Digoxin | 100 in 1 BOTTLE | TABLET | 100 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-2464 | DIGOXIN TABLET [BRYANT RANCH PREPACK] | 100 | Current NDC, 2 package rows | 20240906_03612934-62f4-4002-85af-6c66cd172acb.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 |
|---|
| 71335-2464-1 | 71335246401 | 1000 TABLET in 1 BOTTLE (71335-2464-1) | 1000 tablet | 2024-09-04 | No | No | Historical |
| 71335-2464-2 | 71335246402 | 100 TABLET in 1 BOTTLE (71335-2464-2) | 100 tablet | 2024-09-04 | No | No | Historical |