Warfarin Sodium
- Product NDC
- 65162-767
- 11-digit product format
- 651620767
- Labeler code
- 65162
- Product ID
- 65162-767_55689f10-365b-449e-b224-52363f835529
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals LLC
- Application
- ANDA202202
- Marketing category
- ANDA
- Marketing start
- 2010-08-16
- Substance
- WARFARIN SODIUM
- Active strength
- 6 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
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| WARFARIN SODIUM | 6 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 |
|---|
| 65162-767-10 | Warfarin Sodium | 100 in 1 BOTTLE | TABLET | 100 | | 19 |
| 65162-767-11 | Warfarin Sodium | 1000 in 1 BOTTLE | TABLET | 1000 | | 19 |
| 65162-767-50 | Warfarin Sodium | 500 in 1 BOTTLE | TABLET | 500 | | 19 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| WARFARIN SODIUM | ACTIVE INGREDIENT | 6153CWM0CL | WARFARIN SODIUM (WARFARIN) TABLET [AMNEAL PHARMACEUTICALS, LLC] | 7 | |
| WARFARIN | ACTIVE MOIETY | 5Q7ZVV76EI | WARFARIN SODIUM (WARFARIN) TABLET [AMNEAL PHARMACEUTICALS, LLC] | 7 | |
| D&C RED NO. 6 | INACTIVE INGREDIENT | 481744AI4O | WARFARIN SODIUM (WARFARIN) TABLET [AMNEAL PHARMACEUTICALS, LLC] | 7 | |
| D&C YELLOW NO. 10 | INACTIVE INGREDIENT | 35SW5USQ3G | WARFARIN SODIUM (WARFARIN) TABLET [AMNEAL PHARMACEUTICALS, LLC] | 7 | |
| FD&C BLUE NO. 1 | INACTIVE INGREDIENT | H3R47K3TBD | WARFARIN SODIUM (WARFARIN) TABLET [AMNEAL PHARMACEUTICALS, LLC] | 7 | |
| FD&C BLUE NO. 2 | INACTIVE INGREDIENT | L06K8R7DQK | WARFARIN SODIUM (WARFARIN) TABLET [AMNEAL PHARMACEUTICALS, LLC] | 7 | |
| FD&C RED NO. 40 | INACTIVE INGREDIENT | WZB9127XOA | WARFARIN SODIUM (WARFARIN) TABLET [AMNEAL PHARMACEUTICALS, LLC] | 7 | |
| FD&C YELLOW NO. 6 | INACTIVE INGREDIENT | H77VEI93A8 | WARFARIN SODIUM (WARFARIN) TABLET [AMNEAL PHARMACEUTICALS, LLC] | 7 | |
| HYDROXYPROPYL CELLULOSE (TYPE E) | INACTIVE INGREDIENT | 66O7AQV0RT | WARFARIN SODIUM (WARFARIN) TABLET [AMNEAL PHARMACEUTICALS, LLC] | 7 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | WARFARIN SODIUM (WARFARIN) TABLET [AMNEAL PHARMACEUTICALS, LLC] | 7 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | WARFARIN SODIUM (WARFARIN) TABLET [AMNEAL PHARMACEUTICALS, LLC] | 7 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | WARFARIN SODIUM (WARFARIN) TABLET [AMNEAL PHARMACEUTICALS, LLC] | 7 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65162-767 | WARFARIN SODIUM (WARFARIN) TABLET [AMNEAL PHARMACEUTICALS LLC] | 19 | Current NDC, Legacy NDC, 3 package rows | 20241031_558b7a0d-5490-4c1b-802e-3ab3f1efe760.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 |
|---|
| 65162-767-10 | 65162076710 | 100 TABLET in 1 BOTTLE (65162-767-10) | 100 tablet | 2010-08-16 | 0000-00-00 | No | No | Current |
| 65162-767-11 | 65162076711 | 1000 TABLET in 1 BOTTLE (65162-767-11) | 1000 tablet | 2010-08-16 | 0000-00-00 | No | No | Current |
| 65162-767-50 | 65162076750 | 500 TABLET in 1 BOTTLE (65162-767-50) | 500 tablet | 2010-08-16 | 0000-00-00 | No | No | Current |