Warfarin Sodium
- Product NDC
- 71610-490
- 11-digit product format
- 716100490
- Labeler code
- 71610
- Product ID
- 71610-490_4d6b79ef-a2c8-4fdb-9b0b-0c050ac22b89
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA090935
- Marketing category
- ANDA
- Marketing start
- 2011-05-25
- 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 |
|---|
| 71610-490-30 | 71610049030 | 30 TABLET in 1 BOTTLE (71610-490-30) | 30 tablet | 2020-11-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Warfarin Sodium | Aphena Pharma Solutions - Tennessee, LLC | 2020-12-15 | HUMAN PRESCRIPTION DRUG LABEL | 1 |