WARFARIN SODIUM
- Product NDC
- 72189-210
- 11-digit product format
- 721890210
- Labeler code
- 72189
- Product ID
- 72189-210_2be9877c-0b1d-23b4-e063-6394a90af68f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- WARFARIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA090935
- Marketing category
- ANDA
- Marketing start
- 2021-05-04
- Substance
- WARFARIN SODIUM
- Active strength
- 10 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- WARFARIN SODIUM
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| WARFARIN SODIUM | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6153CWM0CL |
| Rxcui | 855296 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-210-71 | WARFARIN SODIUM | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-210 | WARFARIN SODIUM TABLET [DIRECT RX] | 2 | Current NDC, Legacy NDC, 1 package rows | 20250119_c186d1ff-64dd-bfcb-e053-2a95a90af800.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72189-210-71 | 72189021071 | 100 TABLET in 1 BOTTLE (72189-210-71) | 100 tablet | 2021-05-04 | 0000-00-00 | No | No | Current |