LANOXIN
- Product NDC
- 59212-245
- 11-digit product format
- 592120245
- Labeler code
- 59212
- Product ID
- 59212-245_cf61c0cc-0c5d-46b0-ad21-62bda8e75ea7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Concordia Pharmaceuticals Inc.
- Application
- NDA020405
- Marketing category
- NDA
- Marketing start
- 2012-09-30
- Marketing end
- 2019-09-30
- Substance
- DIGOXIN
- Active strength
- 0 mg/1
- Pharmacologic classes
- Cardiac Glycoside [EPC],Cardiac Glycosides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59212-245-55 | LANOXIN | 100 in 1 BOTTLE | TABLET | 100 | | 12 |
| 59212-245-75 | LANOXIN | 1000 in 1 BOTTLE | TABLET | 1000 | | 12 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59212-245 | LANOXIN (DIGOXIN) TABLET [ADVANZ PHARMA (US) CORP.] | 12 | Legacy NDC, 2 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 | Status |
|---|
| 59212-245-55 | 59212024555 | 100 in 1 BOTTLE | Historical |
| 59212-245-75 | 59212024575 | 1000 in 1 BOTTLE | Historical |