Warfarin Sodium
- Product NDC
- 71335-1786
- 11-digit product format
- 713351786
- Labeler code
- 71335
- Product ID
- 71335-1786_1819dbea-9186-4da0-9000-2970c7fa9819
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202202
- Marketing category
- ANDA
- Marketing start
- 2010-08-16
- Substance
- WARFARIN SODIUM
- Active strength
- 3 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 |
|---|
| 71335-1786-1 | 71335178601 | 90 TABLET in 1 BOTTLE (71335-1786-1) | 90 tablet | 2021-02-23 | No | No | Historical |
| 71335-1786-2 | 71335178602 | 100 TABLET in 1 BOTTLE (71335-1786-2) | 100 tablet | 2021-02-23 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Warfarin Sodium | Bryant Ranch Prepack | 2023-04-12 | HUMAN PRESCRIPTION DRUG LABEL | 103 |