Warfarin Sodium
- Product NDC
- 63629-8843
- 11-digit product format
- 636298843
- Labeler code
- 63629
- Product ID
- 63629-8843_5d9a7cb2-1030-4aba-90f9-0baf4043d1e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040616
- Marketing category
- ANDA
- Marketing start
- 2015-04-07
- Substance
- WARFARIN SODIUM
- Active strength
- 5 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 |
|---|
| 63629-8843-1 | 63629884301 | 100 TABLET in 1 BOTTLE (63629-8843-1) | 100 tablet | 2021-09-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Warfarin Sodium | Bryant Ranch Prepack | 2025-08-20 | HUMAN PRESCRIPTION DRUG LABEL | 103 |