Warfarin Sodium
- Product NDC
- 70518-0279
- 11-digit product format
- 705180279
- Labeler code
- 70518
- Product ID
- 70518-0279_e1051755-24d7-c379-e053-2a95a90a2db7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Warfarin Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040616
- Marketing category
- ANDA
- Marketing start
- 2017-08-02
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0279-0 | 70518027900 | 30 TABLET in 1 BLISTER PACK (70518-0279-0) | 30 tablet | 2017-08-02 | 0000-00-00 | No | No | Current |