Warfarin Sodium
- Product NDC
- 50090-7229
- 11-digit product format
- 500907229
- Labeler code
- 50090
- Product ID
- 50090-7229_ac7348bc-ddb8-46b8-a067-2c7d5cbef379
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040616
- Marketing category
- ANDA
- Marketing start
- 2015-05-12
- 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 |
|---|
| 50090-7229-0 | Warfarin Sodium | 30 in 1 BOTTLE | TABLET | 30 | | 17 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-7229 | WARFARIN SODIUM TABLET [A-S MEDICATION SOLUTIONS] | 17 | Current NDC, 1 package rows | 20240827_5a7d347b-391e-4e9b-a691-1962c7da4fc7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7229-0 | 50090722900 | 30 TABLET in 1 BOTTLE (50090-7229-0) | 30 tablet | 2024-08-23 | No | No | Historical |