LANOXIN
- Product NDC
- 59212-240
- 11-digit product format
- 592120240
- Labeler code
- 59212
- Product ID
- 59212-240_3a39029f-2e63-4894-8a0d-45e122f5047b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Advanz Pharma (US) Corp.
- Application
- NDA020405
- Marketing category
- NDA
- Marketing start
- 2012-09-30
- Substance
- DIGOXIN
- Active strength
- .0625 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
- LANOXIN
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIGOXIN | .0625 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 73K4184T59 |
| Rxcui | 104206, 197604, 197606, 245273, 309888, 309889, 1441565, 1441567 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59212-240-55 | LANOXIN | 100 in 1 BOTTLE | TABLET | 100 | | 12 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59212-240 | LANOXIN (DIGOXIN) TABLET [ADVANZ PHARMA (US) CORP.] | 12 | Current NDC, Legacy NDC, 1 package rows | 20250109_d91e3646-4c63-4512-ab22-db39c085c4dc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59212-240-55 | 59212024055 | 100 TABLET in 1 BOTTLE (59212-240-55) | 100 tablet | 2012-09-30 | 0000-00-00 | No | No | Current |