Warfarin Sodium
- Product NDC
- 50090-7464
- 11-digit product format
- 500907464
- Labeler code
- 50090
- Product ID
- 50090-7464_b49cb9cd-efdd-4c66-9384-0353562b83e9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040616
- Marketing category
- ANDA
- Marketing start
- 2015-05-05
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6153CWM0CL | WARFARIN SODIUM | 129-06-6 | WARFARIN SODIUM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7464-0 | 50090746400 | 30 TABLET in 1 BOTTLE (50090-7464-0) | 30 tablet | 2024-11-20 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Warfarin Sodium | A-S Medication Solutions | 2024-12-24 | HUMAN PRESCRIPTION DRUG LABEL | 22 |