Digox
- Product NDC
- 50090-0962
- 11-digit product format
- 500900962
- Labeler code
- 50090
- Product ID
- 50090-0962_9f46b756-35e0-463d-990b-cbfd265bca1a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Digoxin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076268
- Marketing category
- ANDA
- Marketing start
- 2002-07-26
- Marketing end
- 0000-00-00
- Substance
- DIGOXIN
- Active strength
- 250 ug/1
- Pharmacologic classes
- Cardiac Glycoside [EPC],Cardiac Glycosides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-0962-1 | Digox | 100 in 1 BOTTLE | TABLET | 100 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0962 | DIGOX (DIGOXIN) TABLET [A-S MEDICATION SOLUTIONS] | 6 | Legacy NDC, 1 package rows | 20190225_7b64ac77-71a5-47e3-976e-9b5d7f7eb530.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-0962-1 | 50090096201 | 100 in 1 BOTTLE | Historical |