Warfarin Sodium
- Product NDC
- 71610-589
- 11-digit product format
- 716100589
- Labeler code
- 71610
- Product ID
- 71610-589_3673e690-2fb5-4235-94a8-dd46c7cee8b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA040301
- Marketing category
- ANDA
- Marketing start
- 1999-07-15
- 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 |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71610-589-30 | 71610058930 | 30 TABLET in 1 BOTTLE (71610-589-30) | 30 tablet | 2021-08-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Warfarin Sodium | Aphena Pharma Solutions - Tennessee, LLC | 2021-08-17 | HUMAN PRESCRIPTION DRUG LABEL | 1 |