Warfarin Sodium
- Product NDC
- 0093-1715
- 11-digit product format
- 000931715
- Labeler code
- 0093
- Product ID
- 0093-1715_b8c33971-54b3-4971-bf7f-1bec66999a29
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA040616
- Marketing category
- ANDA
- Marketing start
- 2015-07-14
- 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
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 | 3 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6153CWM0CL |
| Rxcui | 855288, 855296, 855302, 855312, 855318, 855324, 855332, 855338, 855344 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0093-1715-01 | Warfarin Sodium | 100 in 1 BOTTLE | TABLET | 100 | | 20 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0093-1715 | WARFARIN SODIUM TABLET [TEVA PHARMACEUTICALS USA, INC.] | 18 | Current NDC, Legacy NDC, 1 package rows | 20221014_0cbce382-9c88-4f58-ae0f-532a841e8f95.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 |
|---|
| 0093-1715-01 | 00093171501 | 100 TABLET in 1 BOTTLE (0093-1715-01) | 100 tablet | 2015-07-14 | 0000-00-00 | No | No | Current |