Warfarin Sodium
- Product NDC
- 51655-993
- 11-digit product format
- 516550993
- Labeler code
- 51655
- Product ID
- 51655-993_4bcf808c-64ca-a1d3-e063-6294a90adc62
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA040616
- Marketing category
- ANDA
- Marketing start
- 2023-03-29
- 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
- 2027-12-31
- 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 |
|---|
| 51655-993-52 | 51655099352 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-993-52) | 30 tablet | 2023-03-29 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Warfarin Sodium | Northwind Health Company, LLC | 2026-01-01 | HUMAN PRESCRIPTION DRUG LABEL | 4 |