Warfarin Sodium
- Product NDC
- 17856-4034
- 11-digit product format
- 178564034
- Labeler code
- 17856
- Product ID
- 17856-4034_d810d82f-86d3-4674-b5fb-fa4f6ba28e6e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- ANDA040301
- Marketing category
- ANDA
- Marketing start
- 2018-11-19
- Marketing end
- 0000-00-00
- Substance
- WARFARIN SODIUM
- Active strength
- 8 mg/1
- Pharmacologic classes
- Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17856-4034-1 | Warfarin Sodium | 100 in 1 BOX, UNIT-DOSE | TABLET | 100 | | 1 |
| 17856-4034-1 | Warfarin Sodium | 1 in 1 POUCH | TABLET | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-4034 | WARFARIN SODIUM TABLET [ATLANTIC BIOLOGICALS CORP.] | 1 | Legacy NDC, 2 package rows | 20181120_06b0fad4-fb3d-497f-8bf1-8d8a79ac4164.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 17856-4034-1 | 17856403401 | 100 in 1 BOX, UNIT-DOSE | Historical |