Warfarin Sodium
- Product NDC
- 70518-4637
- 11-digit product format
- 705184637
- Labeler code
- 70518
- Product ID
- 70518-4637_5074cf6c-93ed-43e0-e063-6394a90a7c32
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040301
- Marketing category
- ANDA
- Marketing start
- 2026-04-26
- Substance
- WARFARIN SODIUM
- Active strength
- 1 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 | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6153CWM0CL |
| Rxcui | 855288 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4637-0 | Warfarin Sodium | 50 in 1 BOX | TABLET | 50 | | 1 |
| 70518-4637-1 | Warfarin Sodium | 1 in 1 POUCH | TABLET | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4637-0 | 70518463700 | 50 POUCH in 1 BOX (70518-4637-0) / 1 TABLET in 1 POUCH (70518-4637-1) | 50 pouch | 2026-04-26 | No | No | Historical |
| 70518-4637-1 | 70518463701 | 1 in 1 POUCH | | | | | Historical |