Digoxin
- Product NDC
- 72162-2269
- 11-digit product format
- 721622269
- Labeler code
- 72162
- Product ID
- 72162-2269_be6f84d6-d95b-4e39-8c32-26176f5c98ef
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Digoxin
- Listing expiration
- 2027-12-31
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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2269 | DIGOXIN TABLET [BRYANT RANCH PREPACK] | 103 | Current NDC, 4 package rows | 20240810_dcf9b23b-5840-46ff-bb61-c57a02831a03.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 |
|---|
| 72162-2269-0 | 72162226900 | 1000 TABLET in 1 BOTTLE (72162-2269-0) | 1000 tablet | 2024-02-21 | No | No | Historical |
| 72162-2269-1 | 72162226901 | 100 TABLET in 1 BOTTLE (72162-2269-1) | 100 tablet | 2024-02-21 | No | No | Historical |
| 72162-2269-2 | 72162226902 | 1000 TABLET in 1 BOTTLE (72162-2269-2) | 1000 tablet | 2024-02-21 | No | No | Historical |
| 72162-2269-4 | 72162226904 | 100 TABLET in 1 BOTTLE (72162-2269-4) | 100 tablet | 2024-02-21 | No | No | Historical |