Warfarin Sodium
- Product NDC
- 50090-2035
- 11-digit product format
- 500902035
- Labeler code
- 50090
- Product ID
- 50090-2035_96883ebd-1852-46b6-a0e7-8b9c7086a61e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090935
- Marketing category
- ANDA
- Marketing start
- 2011-11-01
- Marketing end
- 0000-00-00
- Substance
- WARFARIN SODIUM
- Active strength
- 2 mg/1
- Pharmacologic classes
- Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2035 | WARFARIN SODIUM TABLET WARFARIN SODIUM TABLET [A-S MEDICATION SOLUTIONS] | 18 | Legacy NDC | 20230429_41c21e36-b1d5-4697-9c0d-ca023932524f.zip |