Warfarin Sodium
- Product NDC
- 51655-993
- 11-digit product format
- 516550993
- Labeler code
- 51655
- Product ID
- 51655-993_4bcf808c-64ca-a1d3-e063-6294a90adc62
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA040616
- Marketing category
- ANDA
- Marketing start
- 2023-03-29
- Substance
- WARFARIN SODIUM
- Active strength
- 2 mg/1
- Pharmacologic classes
- Vitamin K Antagonist [EPC], Vitamin K Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Warfarin Sodium
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| WARFARIN SODIUM | 2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6153CWM0CL |
| Rxcui | 855302 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51655-993-52 | Warfarin Sodium | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-993 | WARFARIN SODIUM TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 1 | Current NDC, 1 package rows | 20230404_f86fe457-a1b6-e54d-e053-6294a90a9bc7.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 |
|---|
| 51655-993-52 | 51655099352 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-993-52) | 30 tablet | 2023-03-29 | No | No | Current |