Warfarin Sodium
- Product NDC
- 67046-1463
- 11-digit product format
- 670461463
- Labeler code
- 67046
- Product ID
- 67046-1463_2d58d9b1-2c04-42e2-e063-6294a90a205c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Coupler LLC
- Application
- ANDA202202
- Marketing category
- ANDA
- Marketing start
- 2025-02-04
- Substance
- WARFARIN SODIUM
- Active strength
- 4 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 |
| 5Q7ZVV76EI | WARFARIN | 81-81-2 | Warfarin |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67046-1463-3 | 67046146303 | 30 TABLET in 1 BLISTER PACK (67046-1463-3) | 30 tablet | 2025-02-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Warfarin Sodium | Coupler LLC | 2025-02-04 | HUMAN PRESCRIPTION DRUG LABEL | 1 |